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US20150376717A1 - Methods and kits for detecting melanoma - Google Patents

Methods and kits for detecting melanoma Download PDF

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US20150376717A1
US20150376717A1 US14/789,543 US201514789543A US2015376717A1 US 20150376717 A1 US20150376717 A1 US 20150376717A1 US 201514789543 A US201514789543 A US 201514789543A US 2015376717 A1 US2015376717 A1 US 2015376717A1
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methylation
melanoma
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methylated
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Nancy Thomas
Kathleen Dorsey
Sharon Edmiston
Pamela Groben
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University of North Carolina at Chapel Hill
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    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
    • C12Q1/6886—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
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    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
    • G01N33/6881—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids from skin
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    • C12Q2600/00—Oligonucleotides characterized by their use
    • C12Q2600/154—Methylation markers
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    • C12Q2600/00—Oligonucleotides characterized by their use
    • C12Q2600/156—Polymorphic or mutational markers
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    • C12Q2600/00—Oligonucleotides characterized by their use
    • C12Q2600/16—Primer sets for multiplex assays

Definitions

  • This invention relates generally to the discovery of novel differentially methylated regulatory elements associated with melanoma.
  • the invention provides methods for detecting melanoma, related kits, and methods of screening for compounds to prevent or treat melanoma.
  • Skin cancer is the most common form of cancer.
  • keratinocyte cancers basic and squamous cell carcinomas
  • melanoma is less than five percent of the skin cancers, it is the seventh most common malignancy in the U.S. and is responsible for most of the skin cancer related deaths.
  • the American Cancer Society estimates that in the U.S. 114,000 new cases of melanoma, including 68,000 invasive and 46,000 noninvasive melanomas, will be diagnosed in 2010 and almost 9,000 people will die of melanoma (Jemal et al., CA Cancer J. Clin. 2010 July 7 [Epub ahead of print]).
  • the WHO estimates that 48,000 people die worldwide of melanoma every year (Lucas, R., Global Burden of Disease of Solar Ultraviolet Radiation, Environmental Burden of Disease Series , Jul. 25, 2006; No. 13. News release, World Health Organization).
  • the clinical outcome for melanoma depends on the stage at the time of the initial diagnosis.
  • the prognosis is good.
  • it is a deadly disease.
  • the ACS reports that the 5-year survival rate is 92% for melanoma diagnosed when small and localized, stage IA or IB.
  • the 5-year survival rate drops to 15-20% for distant metastatic disease, or stage IV melanoma. It is therefore imperative to diagnose melanoma in its earliest form.
  • nevi especially atypical or dysplastic nevi
  • atypical or dysplastic nevi are difficult to distinguish from melanoma, even by expert pathologists (Farmer et al., 1996, Hum. Pathol. 27, 528-531).
  • the numbers involved are substantial in the U.S. alone.
  • NCCN Clin. Pract. Guidelines in Oncology—v. 2.2010 : Melanoma , Mar. 17, 2010, page ME-B).
  • excisional biopsy with such broad margins may not be appropriate for sites such as the face, ears, fingers, palms, or soles of the feet.
  • Better histopathology will improve the ability for doctors to choose the appropriate intervention, such as margin controlled surgery (Mohs surgery) with 0.2 cm margins.
  • IHC is often used as an adjunct to the standard histopathologic examination (hematoxylin and eosin (H&E) staining, etc.) for melanocytic lesions or to determine the tumor of origin.
  • Antibodies such as 5100, HMB-45, Ki-67 (MIB1), MITF and MART-1/Melan-A or cocktails of several may be used for staining (Ivan & Prieto, 2010, Future Oncol. 6(7), 1163-1175; Linos et al., 2011, Biomarkers Med. 5(3) 333-360).
  • melanoma cell adhesion molecule MCAM
  • MUC18 matrix metalloproteinase-2
  • Ki-67 proliferating cell nuclear antigen
  • PCNA proliferating cell nuclear antigen
  • p16/INK4A melanoma cell adhesion molecule
  • Rothberg et al. also note that these and other “molecular prognostic markers have largely failed to be incorporated into guidelines, staging systems, or the standard of care for melanoma patients.”
  • CT cross sectional imaging
  • MRI magnetic resonance imaging
  • PET magnetic resonance imaging
  • NCL serum lactate dehydrogenase
  • stage III complete lymph dissection may be indicated.
  • stage III complete lymph dissection may be indicated.
  • stage III complete lymph dissection may be indicated.
  • stage III complete lymph dissection may be indicated.
  • stage III complete lymph dissection may be indicated.
  • stage III complete lymph dissection may be indicated.
  • stage III complete lymph dissection may be indicated.
  • stage III complete lymph dissection may be indicated.
  • stage III complete lymph dissection may be indicated.
  • stage JIB or III melanoma some studies have shown that adjuvant interferon alfa has led to longer disease free survival.
  • first- or second-line stage III and IV melanoma systemic treatments include: carboplatin, cisplatin, dacarbazine, interferon alfa, high-dose interleukin-2, paclitaxel, temozolomide, vinblastine or combinations thereof (NCCN Guidelines, ME-D, MS-9-13).
  • Riker et al. report gene expression profiles of primary and metastatic melanomas (Riker et al., 2008, BMC Med. Genomics, 1, 13, pub. 28 Apr. 2008).
  • FISH fluorescence in situ hybridization
  • DNA methylation may provide a tool, in conjunction with histopathology, for the molecular diagnostics of melanoma.
  • DNA methylation is an epigenetic chemical modification that does not alter the sequence code, but can be heritable, and is involved in the regulation of gene expression (Plass, 2002, Hum. Mol. Genet. 11, 2479-2488).
  • the most common methylation site in mammals is a cytosine located next to a guanosine (CpG).
  • Clusters of CpGs, referred to as islands, are found in the 5′ regulatory and promoter regions of genes (Antequera and Bird, 1993, Proc. Natl. Acad. Sci. USA, 90, 11995-11999).
  • Hypermethylation of CpG islands in promoter regions is a common mechanism of tumor suppressor gene silencing in cancer (Balmain et al., 2003, Nat. Genet. 33 Suppl, 238-244; Baylin and Herman, 2000, Trends Genet. 16, 168-174; Feinberg and Tycko, 2004, Nat. Rev. Cancer 4, 143-153; Plass, 2002).
  • Aberrant promoter methylation with silencing of tumor suppressor genes has been shown to occur widely in human melanomas (Furuta et al., 2004, Cancer Sci.
  • melanoma Molecular diagnosis of melanoma holds promise but, due to the small size of melanocytic lesions which are typically submitted in entirety for diagnosis, any new diagnostic tests need to be valid and reproducible in FFPE tissues.
  • gene expression arrays were used to identify markers of melanoma heterogeneity using cell lines and a few frozen and FFPE melanomas, but found that only 24% of unselected FFPE samples produced RNA of sufficient quality for microarray analysis (Penland et al., 2007 , Lab. Invest. 87, 383-391). Improvements in melanoma diagnosis could be accelerated by the use of molecular assays that are less sensitive to tissue fixation than RNA-based assays. Moreover, there is an unmet medical need for improved melanoma diagnosis. The invention described herein provides a solution.
  • the present invention provides a method for detecting melanoma in a tissue sample which comprises: (a) measuring a level of methylation of one or more regulatory elements differentially methylated in melanoma and benign nevi; and (b) determining whether melanoma is present or absent in the tissue sample.
  • the methylation may be measured at single CpG site resolution.
  • the tissue sample may be a common nevi, a dysplastic nevi, or a benign atypical nevi sample, or a melanocytic lesion of unknown potential.
  • the sample may be prepared in a variety of ways including, but not limited to, a formalin-fixed, paraffin-embedded (FFPE) sample, a fresh-frozen sample, or a fresh tissue sample.
  • FFPE formalin-fixed, paraffin-embedded
  • a fresh-frozen sample or a fresh tissue sample.
  • FFPE formalin-fixed, paraffin-embedded
  • the samples including but not limited to, dissected tissue, an excision biopsy, a needle biopsy, a punch biopsy, a shave biopsy, a tape biopsy, or a skin biopsy.
  • the sample may be from a lymph node biopsy, a sentinel lymph node, or a cancer metastasis.
  • the present invention provides that the differentially methylatated regulatory elements are elements associated with immune response/inflammatory pathway genes, hormonal regulation genes, or cell growth/cell adhesion/apoptosis genes.
  • the regulatory elements may be associated with a gene encoding CARD15, CCL3, CD2, EMR3, EVI2A, FRZB, GSTM2, HLA-DPA1, IFNG, ITK, KCNK4, KLK10, LAT, MPO, NPR2, OSM, PSCA, PTHLH, PTHR1, RUNX3, TNFSF8 or TRIP6.
  • hypermethylation of the regulatory elements associated with a gene encoding FRZB, GSTM2, KCNK4, NPR2, or TRIP6 is indicative of melanoma.
  • hypomethylation of the regulatory elements associated with a gene encoding CARD15, CCL3, CD2, EMR3, EVI2A, HLA-DPA1, IFNG, ITK, KLK10, LAT, MPO, OSM, PSCA, PTHLH, PTHR1, RUNX3 or TNFSF8 is indicative of melanoma.
  • a panel of 22 genes is used.
  • a panel of 14 genes is used.
  • the level of methylation may be measured using a variety of methods including, but not limited to, assays based on bisulfate conversion-based microarray, differential hybridization, methylated DNA immunoprecipitation, methylated CpG island recovery (MIRA), methylation specific polymerase chain reaction (MSP), or methylation-sensitive high resolution melting (MS-HRM).
  • the detection of the differentially methylated elements may also be by microarray or mass spectrometry.
  • the differentially methylated elements may be amplified by pyrosequencing, invasive cleavage amplification, sequencing by ligation, or emulsion-based PCR.
  • the regulatory element differentially methylated has a sensitivity analysis area under the curve of greater than 0.70, 0.75, 0.8, 0.85, 0.9, 0.95, 0.98, or 0.99.
  • the levels of methylation for 4 or more regulatory elements may be measured. Alternatively, 8 or 12 or more regulatory elements are measured.
  • the method further comprises evaluating the quality of the sample by measuring the levels of skin specific markers using antibody staining, differential methylation, expression analysis, or fluorescence in situ hybridization (FISH).
  • FISH fluorescence in situ hybridization
  • the methods of the present invention may also include staining the tissue sample with one or more antibodies specific for melanoma.
  • the antibody may be S100, gp100 (HMB-45 antibody), MART-1/Melan-A, MITF, or tyrosinase antibodies, or a cocktail of all three antibodies.
  • the methods may further comprise fluorescence in situ hybridization (FISH), comparative genomic hybridization (CGH), or gene expression analysis.
  • the invention also includes measuring transcription of genes or the translation of proteins that are indirectly or directly under the influence of a gene hyper- or hypomethylated in melanoma.
  • the invention includes using antibodies or probes or primers to measure FRZB, GSTM2, KCNK4, NPR2, or TRIP6 proteins or nucleic acids, wherein reduced levels are indicative of melanoma.
  • the levels relative to a benign control may be about 80%, preferably 50%, more preferably 25-0%.
  • the levels relative to a benign control may be 110%, more preferably 150%, more preferably 200-500% (i.e., two to five fold higher relative to the control), more preferably 1000-3000% higher.
  • the present invention provides a kit comprising: (a) at least one reagent selected from the group consisting of: (i) a nucleic acid probe capable of specifically hybridizing with a regulatory element differentially methylated in melanoma and benign nevi; (ii) a pair of nucleic acid primers capable of PCR amplification of a regulatory element differentially methylated in melanoma and benign nevi; and (iii) a methylation specific antibody and a probe capable of specifically hybridizing with a regulatory element differentially methylated in melanoma and benign nevi; and (b) instructions for use in measuring a level of methylation of at least one regulatory element in a tissue sample from a subject suspected of having melanoma.
  • the present invention provides a method of identifying a compound that prevents or treats melanoma progression, the method comprising the steps of: (a) contacting a compound with a sample comprising a cell or a tissue; (b) measuring a level of methylation of one or more regulatory elements differentially methylated in melanoma and benign nevi; and (c) determining a functional effect of the compound on the level of methylation; thereby identifying a compound that prevents or treats melanoma.
  • FIGS. 1A-1I show correlation curves showing the reproducibility and effects of formalin fixation and normal cell contamination on melanocytic methylation profiles obtained with the Illumina GoldenGate methylation array.
  • FIGS. 1A-1I show correlation curves showing the reproducibility and effects of formalin fixation and normal cell contamination on melanocytic methylation profiles obtained with the Illumina GoldenGate methylation array.
  • FIGS. 1A-1C show the reproducibility and effects of formalin fixation on methylation profile. Shown are non
  • 1D-II show the effect of contamination with increasing proportions of normal peripheral blood leukocyte (PBL) DNA on the Mel-505 melanoma cell methylation profile. Shown are Mel-505 cells that were mixed with PBL DNA in the following proportions: 100% Mel-505, ( FIG. 1D ); 90% Mel-505/10% PBL ( FIG. 1E ); 80% Mel-505/20% PBL ( FIG. 1F ); 70% Mel-505/30% PBL ( FIG. 1G ); 60% Mel-505/40% PBL ( FIG. 1H ); and 50% Mel-505/50% PBL ( FIG. 1I ).
  • PBL peripheral blood leukocyte
  • FIGS. 2A and 2B show the hierarchical clustering of methylation ⁇ values using the Illumina GoldenGate Cancer Panel I array in FFPE benign nevi and malignant melanomas. DNA methylation profiles for 22 melanomas and 27 nevi are shown. Columns represent tissue samples; rows represent CpG loci. The methylation levels ( ⁇ ) range from 0 (very light grey/unmethylated) to 1 (dark grey/highly methylated). Missing values are shown in white.
  • FIGS. 2A and 2B display clusters based on the 29 CpG sites/genes showing significantly different methylation ⁇ levels between moles and melanomas after adjustment for age and sex and Bonferroni correction for multiple comparisons. The upper portion of the heatmap shows 7 CpG loci in 6 genes exhibiting hypermethylation and 22 CpG loci in 18 genes exhibiting hypomethylation in melanomas compared with moles.
  • FIGS. 3A-3L show box plots of methylation ⁇ levels in the 12 CpG loci identified by PAM analysis that predict melanoma.
  • the loci shown differed by >0.2 mean ⁇ between melanomas and moles, except for ITK_P114_F.
  • Each box plot shows the mean ⁇ value (dark bar within box), the standard deviation (outer boundaries of box), and the range of ⁇ values (broken line) within the melanomas or nevus groups. Additional information on mean ⁇ values for nevi and melanomas, differences in mean ⁇ values, and p-values adjusted for age, sex, and multiple comparisons through Bonferroni correction are given in Table 3A.
  • FIG. 4A-4O show ROC curves showing the sensitivity and specificity of selected CpG loci to distinguish melanomas from benign nevi based on methylation level.
  • Sensitivity, or the frequency of detection of true positives (melanoma vs nevus) is shown along the y axis, while specificity, or the frequency of false positives, is shown along the x axis.
  • the calculated AUC is given for each plot.
  • FIG. 5 shows a Venn diagram of CpG sites that significantly differentiate non-dysplastic and dysplastic nevi from primary melanomas or metastases.
  • melanoma refers to malignant neoplasms of melanocytes, which are pigment cells present normally in the epidermis, in adnexal structures including hair follicles, and sometimes in the dermis, as well as extracutaneous sites such as the mucosa, meninx, conjuctiva, and uvea. Sometimes it is referred to as “cutaneous melanoma” or “malignant melanoma.” There are at least four types of cutaneous melanoma: lentigo maligna melanoma (LMM), superficial spreading melanoma (SSM), nodular melanoma (NM), and acral lentiginous melanoma (ALM).
  • LMM lentigo maligna melanoma
  • SSM superficial spreading melanoma
  • NM nodular melanoma
  • ALM acral lentiginous melanoma
  • Cutaneous melanoma typically starts as a proliferation of single melanocytes, e.g., at the junction of the epidermis and the dermis.
  • the cells first grow in a horizontal manner and settle in an area of the skin that can vary from a few millimeters to several centimeters.
  • the transformed melanocytes produce increased amounts of pigment so that the area involved can be seen by the clinician.
  • nucleic acid and “nucleic acid molecule” may be used interchangeably throughout the disclosure.
  • the terms refer to nucleic acids of any composition from, such as DNA (e.g., complementary DNA (cDNA), genomic DNA (gDNA) and the like), RNA (e.g., messenger RNA (mRNA), short inhibitory RNA (siRNA), ribosomal RNA (rRNA), tRNA, microRNA, RNA highly expressed by the melanoma or nevi, and the like), and/or DNA or RNA analogs (e.g., containing base analogs, sugar analogs and/or a non-native backbone and the like), RNA/DNA hybrids and polyamide nucleic acids (PNAs), all of which can be in single- or double-stranded form, and unless otherwise limited, can encompass known analogs of natural nucleotides that can function in a similar manner as naturally occurring nucleotides.
  • DNA e.g., complementary DNA (cDNA), genomic DNA (gDNA
  • nucleic acids examples include SEQ ID Nos. 1-75 shown in Table 4A and Table 4B; SEQ ID Nos. 76-93 in Table 7A and 7B; SEQ ID Nos. 94-265 in Table 9D; SEQ ID Nos. 266-283 in Table 13; SEQ ID Nos. 284-339 in Table 14; and SEQ ID Nos. 340-353 in Table 15, which may be methylated or unmethylated at any CpG site present in the sequence, including the CpG sites shown in brackets on some sequences.
  • a template nucleic acid in some embodiments can be from a single chromosome (e.g., a nucleic acid sample may be from one chromosome of a sample obtained from a diploid organism).
  • nucleic acid Unless specifically limited, the term encompasses nucleic acids containing known analogs of natural nucleotides that have similar binding properties as the reference nucleic acid and are metabolized in a manner similar to naturally occurring nucleotides. Unless otherwise indicated, a particular nucleic acid sequence also implicitly encompasses methylated forms, conservatively modified variants thereof (e.g., degenerate codon substitutions), alleles, orthologs, single nucleotide polymorphisms (SNPs), and complementary sequences as well as the sequence explicitly indicated.
  • nucleic acid is used interchangeably with locus, gene, cDNA, and mRNA encoded by a gene.
  • RNA or DNA synthesized from nucleotide analogs single-stranded (“sense” or “antisense”, “plus” strand or “minus” strand, “forward” reading frame or “reverse” reading frame) and double-stranded polynucleotides.
  • Deoxyribonucleotides include deoxyadenosine, deoxycytidine, deoxyguanosine and deoxythymidine.
  • RNA the base cytosine is replaced with uracil.
  • a “methylated regulatory element” as used herein refers to a segment of DNA sequence at a defined location in the genome of an individual.
  • a “methylated regulatory element” is at least 15 nucleotides in length and contains at least one cytosine. It may be at least 18, 20, 25, 30, 50, 80, 100, 150, 200, 250, or 300 nucleotides in length and contain 1 or 2, 5, 10, 15, 20, 25, or 30 cytosines.
  • nucleotide sequence variations may exist from individual to individual and from allele to allele even for the same individual.
  • such a region centering around a defined genetic locus contains the locus as well as upstream and/or downstream sequences.
  • Each of the upstream or downstream sequence (counting from the 5′ or 3′ boundary of the genetic locus, respectively) can be as long as 10 kb, in other cases may be as long as 5 kb, 2 kb, 1 kb, 500 bp, 200 bp, or 100 bp.
  • a “methylated regulatory element” may modulate expression of a nucleotide sequence transcribed into a protein or not transcribed for protein production (such as a non-coding mRNA).
  • the “methylated regulatory element” may be an inter-gene sequence, intra-gene sequence (intron), protein-coding sequence (exon), a non protein-coding sequence (such as a transcription promoter or enhancer), or a combination thereof.
  • a “methylated nucleotide” or a “methylated nucleotide base” refers to the presence of a methyl moiety on a nucleotide base, where the methyl moiety is not present in a recognized typical nucleotide base.
  • cytosine does not contain a methyl moiety on its pyrimidine ring, but 5-methylcytosine contains a methyl moiety at position 5 of its pyrimidine ring. Therefore, cytosine is not a methylated nucleotide and 5-methylcytosine is a methylated nucleotide.
  • thymine contains a methyl moiety at position 5 of its pyrimidine ring, however, for purposes herein, thymine is not considered a methylated nucleotide when present in DNA since thymine is a typical nucleotide base of DNA.
  • Typical nucleoside bases for DNA are thymine, adenine, cytosine and guanine.
  • Typical bases for RNA are uracil, adenine, cytosine and guanine.
  • a “methylation site” is the location in the target gene nucleic acid region where methylation has, or has the possibility of occurring. For example a location containing CpG is a methylation site wherein the cytosine may or may not be methylated.
  • a “CpG site” or “methylation site” is a nucleotide within a nucleic acid that is susceptible to methylation either by natural occurring events in vivo or by an event instituted to chemically methylate the nucleotide in vitro.
  • a “methylated nucleic acid molecule” refers to a nucleic acid molecule that contains one or more nucleotides that is/are methylated.
  • a “CpG island” as used herein describes a segment of DNA sequence that comprises a functionally or structurally deviated CpG density.
  • Yamada et al. have described a set of standards for determining a CpG island: it must be at least 400 nucleotides in length, has a greater than 50% GC content, and an OCF/ECF ratio greater than 0.6 (Yamada et al., 2004, Genome Research, 14, 247-266).
  • Others have defined a CpG island less stringently as a sequence at least 200 nucleotides in length, having a greater than 50% GC content, and an OCF/ECF ratio greater than 0.6 (Takai et al., 2002 , Proc. Natl. Acad. Sci. USA, 99, 3740-3745).
  • epigenetic state refers to any structural feature at a molecular level of a nucleic acid (e.g., DNA or RNA) other than the primary nucleotide sequence.
  • a nucleic acid e.g., DNA or RNA
  • the epigenetic state of a genomic DNA may include its secondary or tertiary structure determined or influenced by, e.g., its methylation pattern or its association with cellular proteins.
  • methylation profile “methylation state” or “methylation status,” as used herein to describe the state of methylation of a genomic sequence, refers to the characteristics of a DNA segment at a particular genomic locus relevant to methylation. Such characteristics include, but are not limited to, whether any of the cytosine (C) residues within this DNA sequence are methylated, location of methylated C residue(s), percentage of methylated C at any particular stretch of residues, and allelic differences in methylation due to, e.g., difference in the origin of the alleles.
  • methylation profile or “methylation status” also refers to the relative or absolute concentration of methylated C or unmethylated C at any particular stretch of residues in a biological sample.
  • cytosine (C) residue(s) not typically methylated within a DNA sequence are methylated, it may be referred to as “hypermethylated”; whereas if cytosine (C) residue(s) typically methylated within a DNA sequence are not methylated, it may be referred to as “hypomethylated”.
  • the cytosine (C) residue(s) within a DNA sequence e.g., sample nucleic acid
  • the cytosine (C) residue(s) within a DNA sequence are methylated as compared to another sequence from a different region or from a different individual (e.g., relative to normal nucleic acid), that sequence is considered hypermethylated compared to the other sequence.
  • cytosine (C) residue(s) within a DNA sequence are not methylated as compared to another sequence from a different region or from a different individual, that sequence is considered hypomethylated compared to the other sequence.
  • These sequences are said to be “differentially methylated”, and more specifically, when the methylation status differs between melanoma and benign or healthy moles, the sequences are considered “differentially methylated in melanoma and benign nevi”.
  • Measurement of the levels of differential methylation may be done by a variety of ways known to those skilled in the art. One method is to measure the ratio of methylated to unmethylated alleles or ⁇ -value (see section 6.5 below).
  • the difference in the ratios between methylated and unmethylated sequences in melanoma and benign nevi may be 0.1, 0.15, 0.2, 0.25, 0.3, 0.4, 0.5, 0.55, 0.6, 0.65, 0.7, 0.8, or 0.9. In non-limiting embodiments, the difference in the ratios is between 0.2 and 0.65, or between 0.2 and 0.4.
  • agent that binds to methylated nucleotides refers to a substance that is capable of binding to methylated nucleic acid.
  • the agent may be naturally-occurring or synthetic, and may be modified or unmodified. In one embodiment, the agent allows for the separation of different nucleic acid species according to their respective methylation states.
  • An example of an agent that binds to methylated nucleotides is described in PCT Pub. No. WO 2006/056480 A2 (Rehli), hereby incorporated by reference in its entirety.
  • the described agent is a bifunctional polypeptide comprising the DNA-binding domain of a protein belonging to the family of Methyl-CpG binding proteins (MBDs) and an Fc portion of an antibody.
  • MBDs Methyl-CpG binding proteins
  • the recombinant methyl-CpG-binding, antibody-like protein can preferably bind CpG methylated DNA in an antibody-like manner. That means, the methyl-CpG-binding, antibody-like protein has a high affinity and high avidity to its “antigen”, which is preferably DNA that is methylated at CpG dinucleotides.
  • the agent may also be a multivalent MBD.
  • bisulfite encompasses any suitable type of bisulfite, such as sodium bisulfite, or other chemical agent that is capable of chemically converting a cytosine (C) to a uracil (U) without chemically modifying a methylated cytosine and therefore can be used to differentially modify a DNA sequence based on the methylation status of the DNA, e.g., U.S. Pat. Pub. US 2010/0112595 (Menchen et al.).
  • a reagent that “differentially modifies” methylated or non-methylated DNA encompasses any reagent that modifies methylated and/or unmethylated DNA in a process through which distinguishable products result from methylated and non-methylated DNA, thereby allowing the identification of the DNA methylation status.
  • processes may include, but are not limited to, chemical reactions (such as a C ⁇ U conversion by bisulfite) and enzymatic treatment (such as cleavage by a methylation-dependent endonuclease).
  • an enzyme that preferentially cleaves or digests methylated DNA is one capable of cleaving or digesting a DNA molecule at a much higher efficiency when the DNA is methylated, whereas an enzyme that preferentially cleaves or digests unmethylated DNA exhibits a significantly higher efficiency when the DNA is not methylated.
  • non-bisulfite-based method and “non-bisulfite-based quantitative method” as used herein refer to any method for quantifying methylated or non-methylated nucleic acid that does not require the use of bisulfite.
  • the terms also refer to methods for preparing a nucleic acid to be quantified that do not require bisulfite treatment. Examples of non-bisulfite-based methods include, but are not limited to, methods for digesting nucleic acid using one or more methylation sensitive enzymes and methods for separating nucleic acid using agents that bind nucleic acid based on methylation status.
  • methyl-sensitive enzymes and “methylation sensitive restriction enzymes” are DNA restriction endonucleases that are dependent on the methylation state of their DNA recognition site for activity. For example, there are methyl-sensitive enzymes that cleave or digest at their DNA recognition sequence only if it is not methylated. Thus, an unmethylated DNA sample will be cut into smaller fragments than a methylated DNA sample. Similarly, a hypermethylated DNA sample will not be cleaved. In contrast, there are methyl-sensitive enzymes that cleave at their DNA recognition sequence only if it is methylated. As used herein, the terms “cleave”, “cut” and “digest” are used interchangeably.
  • target nucleic acid refers to a nucleic acid examined using the methods disclosed herein to determine if the nucleic acid is melanoma associated.
  • control nucleic acid refers to a nucleic acid used as a reference nucleic acid according to the methods disclosed herein to determine if the nucleic acid is associated with melanoma.
  • gene means the segment of DNA involved in producing a polypeptide chain; it includes regions preceding and following the coding region (leader and trailer) involved in the transcription/translation of the gene product and the regulation of the transcription/translation, as well as intervening sequences (introns) between individual coding segments (exons).
  • polypeptide polypeptide
  • peptide protein
  • proteins proteins
  • amino acid polymers in which one or more amino acid residue is an artificial chemical mimetic of a corresponding naturally occurring amino acid, as well as to naturally occurring amino acid polymers and non-naturally occurring amino acid polymers.
  • the terms encompass amino acid chains of any length, including full-length proteins (i.e., antigens), wherein the amino acid residues are linked by covalent peptide bonds.
  • amino acid refers to naturally occurring and synthetic amino acids, as well as amino acid analogs and amino acid mimetics that function in a manner similar to the naturally occurring amino acids.
  • Naturally occurring amino acids are those encoded by the genetic code, as well as those amino acids that are later modified, e.g., hydroxyproline, gamma-carboxyglutamate, and 0-phosphoserine Amino acids may be referred to herein by either the commonly known three letter symbols or by the one-letter symbols recommended by the IUPAC-IUB Biochemical Nomenclature Commission. Nucleotides, likewise, may be referred to by their commonly accepted single-letter codes.
  • Primers refer to oligonucleotides that can be used in an amplification method, such as a polymerase chain reaction (PCR), to amplify a nucleotide sequence based on the polynucleotide sequence corresponding to a particular genomic sequence, e.g., one specific for a particular CpG site. At least one of the PCR primers for amplification of a polynucleotide sequence is sequence-specific for the sequence.
  • PCR polymerase chain reaction
  • template refers to any nucleic acid molecule that can be used for amplification in the technology. RNA or DNA that is not naturally double stranded can be made into double stranded DNA so as to be used as template DNA. Any double stranded DNA or preparation containing multiple, different double stranded DNA molecules can be used as template DNA to amplify a locus or loci of interest contained in the template DNA.
  • amplification reaction refers to a process for copying nucleic acid one or more times.
  • the method of amplification includes, but is not limited to, polymerase chain reaction, self-sustained sequence reaction, ligase chain reaction, rapid amplification of cDNA ends, polymerase chain reaction and ligase chain reaction, Q-P replicase amplification, strand displacement amplification, rolling circle amplification, or splice overlap extension polymerase chain reaction.
  • a single molecule of nucleic acid may be amplified.
  • sensitivity refers to the number of true positives divided by the number of true positives plus the number of false negatives, where sensitivity (sens) may be within the range of 0 ⁇ sens ⁇ 1.
  • method embodiments herein have the number of false negatives equaling zero or close to equaling zero, so that no subject is wrongly identified as not having melanoma when they indeed have melanoma.
  • an assessment often is made of the ability of a prediction algorithm to classify negatives correctly, a complementary measurement to sensitivity.
  • specificity refers to the number of true negatives divided by the number of true negatives plus the number of false positives, where sensitivity (spec) may be within the range of 0 ⁇ spec ⁇ 1.
  • the methods described herein have the number of false positives equaling zero or close to equaling zero, so that no subject is wrongly identified as having melanoma when they do not in fact have melanoma.
  • a method that has both sensitivity and specificity equaling one, or 100%, is preferred.
  • RNAi molecule refers to a nucleic acid that forms a double stranded RNA, which double stranded RNA has the ability to reduce or inhibit expression of a gene or target gene when the siRNA expressed in the same cell as the gene or target gene.
  • siRNA thus refers to the double stranded RNA formed by the complementary strands.
  • the complementary portions of the siRNA that hybridize to form the double stranded molecule typically have substantial or complete identity.
  • siRNA refers to a nucleic acid that has substantial or complete identity to a target gene and forms a double stranded siRNA.
  • the sequence of the siRNA can correspond to the full length target gene, or a subsequence thereof.
  • the siRNA is at least about 15-50 nucleotides in length (e.g., each complementary sequence of the double stranded siRNA is 15-50 nucleotides in length, and the double stranded siRNA is about 15-50 base pairs in length, preferable about preferably about 20-30 base nucleotides, preferably about 20-25 nucleotides in length, e.g., 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30 nucleotides in length.
  • an “antisense” polynucleotide is a polynucleotide that is substantially complementary to a target polynucleotide and has the ability to specifically hybridize to the target polynucleotide.
  • Ribozymes are enzymatic RNA molecules capable of catalyzing specific cleavage of RNA.
  • the composition of ribozyme molecules preferably includes one or more sequences complementary to a target mRNA, and the well-known catalytic sequence responsible for mRNA cleavage or a functionally equivalent sequence (see, e.g., U.S. Pat. No. 5,093,246 (Cech et al.); U.S. Pat. No.
  • Ribozyme molecules designed to catalytically cleave target mRNA transcripts can also be used to prevent translation of genes associated with the progression of melanoma. These genes may be genes found to be hypomethylated in melanoma.
  • the phrase “functional effects” in the context of assays for testing means compounds that modulate a methylation of a regulatory region of a gene associated with melanoma. This may also be a chemical or phenotypic effect such as altered transcriptional activity of a gene hyper- or hypomethylated in melanoma, or altered activities and the downstream effects of proteins encoded by these genes.
  • a functional effect may include transcriptional activation or repression, the ability of cells to proliferate, expression in cells during melanoma progression, and other characteristics of melanoma cells. “Functional effects” include in vitro, in vivo, and ex vivo activities.
  • determining the functional effect is meant assaying for a compound that increases or decreases the transcription of genes or the translation of proteins that are indirectly or directly under the influence of a gene hyper- or hypomethylated in melanoma.
  • Such functional effects can be measured by any means known to those skilled in the art, e.g., changes in spectroscopic characteristics (e.g., fluorescence, absorbance, refractive index); hydrodynamic (e.g., shape), chromatographic; or solubility properties for the protein; ligand binding assays, e.g., binding to antibodies; measuring inducible markers or transcriptional activation of the marker; measuring changes in enzymatic activity; the ability to increase or decrease cellular proliferation, apoptosis, cell cycle arrest, measuring changes in cell surface markers.
  • spectroscopic characteristics e.g., fluorescence, absorbance, refractive index
  • hydrodynamic e.g., shape
  • solubility properties for the protein ligand binding assays, e.g., binding
  • Validation the functional effect of a compound on melanoma progression can also be performed using assays known to those of skill in the art such as metastasis of melanoma cells by tail vein injection of melanoma cells in mice.
  • the functional effects can be evaluated by many means known to those skilled in the art, e.g., microscopy for quantitative or qualitative measures of alterations in morphological features, measurement of changes in RNA or protein levels for other genes expressed in melanoma cells, measurement of RNA stability, identification of downstream or reporter gene expression (CAT, luciferase, ⁇ -gal, GFP and the like), e.g., via chemiluminescence, fluorescence, colorimetric reactions, antibody binding, inducible markers, etc.
  • CAT reporter gene expression
  • Inhibitors,” “activators,” and “modulators” of the markers are used to refer to activating, inhibitory, or modulating molecules identified using in vitro and in vivo assays of the methylation state, the expression of genes hyper- or hypomethylated in melanoma or the translation proteins encoded thereby Inhibitors, activators, or modulators also include naturally occurring and synthetic ligands, antagonists, agonists, antibodies, peptides, cyclic peptides, nucleic acids, antisense molecules, ribozymes, RNAi molecules, small organic molecules and the like.
  • Such assays for inhibitors and activators include, e.g., (1)(a) measuring methylation states, (b) the mRNA expression, or (c) proteins expressed by genes hyper- or hypomethylated in melanoma in vitro, in cells, or cell extracts; (2) applying putative modulator compounds; and (3) determining the functional effects on activity, as described above.
  • Samples or assays comprising genes hyper- or hypomethylated in melanoma are treated with a potential activator, inhibitor, or modulator are compared to control samples without the inhibitor, activator, or modulator to examine the extent of inhibition.
  • Control samples (untreated with inhibitors) are assigned a relative activity value of 100% Inhibition of methylation, expression, or proteins encoded by genes hyper- or hypomethylated in melanoma is achieved when the activity value relative to the control is about 80%, preferably 50%, more preferably 25-0%.
  • Activation of methylation, expression, or proteins encoded by genes hyper- or hypomethylated in melanoma is achieved when the activity value relative to the control (untreated with activators) is 110%, more preferably 150%, more preferably 200-500% (i.e., two to five fold higher relative to the control), more preferably 1000-3000% higher.
  • test compound or “drug candidate” or “modulator” or grammatical equivalents as used herein describes any molecule, either naturally occurring or synthetic, e.g., protein, oligopeptide, small organic molecule, polysaccharide, peptide, circular peptide, lipid, fatty acid, siRNA, polynucleotide, oligonucleotide, etc., to be tested for the capacity to directly or indirectly modulate genes hyper- or hypomethylated in melanoma.
  • the test compound can be in the form of a library of test compounds, such as a combinatorial or randomized library that provides a sufficient range of diversity.
  • Test compounds are optionally linked to a fusion partner, e.g., targeting compounds, rescue compounds, dimerization compounds, stabilizing compounds, addressable compounds, and other functional moieties.
  • a fusion partner e.g., targeting compounds, rescue compounds, dimerization compounds, stabilizing compounds, addressable compounds, and other functional moieties.
  • new chemical entities with useful properties are generated by identifying a test compound (called a “lead compound”) with some desirable property or activity, e.g., inhibiting activity, creating variants of the lead compound, and evaluating the property and activity of those variant compounds.
  • HTS high throughput screening
  • the compound may be “small organic molecule” that is an organic molecule, either naturally occurring or synthetic, that has a molecular weight of more than about 50 daltons and less than about 2500 daltons, preferably less than about 2000 daltons, preferably between about 100 to about 1000 daltons, more preferably between about 200 to about 500 daltons.
  • the tissue sample may be from a patient suspected of having melanoma or from a patient diagnosed with melanoma, e.g., for confirmation of diagnosis or establishing a clear margin or for the detection of melanoma cells in other tissues such as lymph nodes.
  • the biological sample may also be from a subject with an ambiguous diagnosis in order to clarify the diagnosis.
  • the sample may be obtained for the purpose of differential diagnosis, e.g., a subject with a histopathologically benign lesion to confirm the diagnosis.
  • the sample may also be obtained for the purpose of prognosis, i.e., determining the course of the disease and selecting primary treatment options. Tumor staging and grading are examples of prognosis.
  • the sample may also be evaluated to select or monitor therapy, selecting likely responders in advance from non-responders or monitoring response in the course of therapy.
  • the sample may be evaluated as part of post-treatment ongoing surveillance of patients who have had melanoma.
  • the sample may also be obtained to differentiate dysplastic nevi from other benign nevi.
  • the sample may be a melanoma sample such as a melanomas will be superficial spreading melanoma, nodular melanoma, lentigo maligna melanoma, acral lentiginous melanoma, unclassifiable or other (spitzoid/desmoplastic/nevoid/spindle cell) melanoma.
  • the sample may be normal skin, a benign nevi, a melanoma-in-situs (MIS), or a high-grade dysplastic nevi (HGDN).
  • Bio samples may be obtained using any of a number of methods in the art.
  • biological samples comprising potential melanocytic lesions include those obtained from excised skin biopsies, such as punch biopsies, shave biopsies, fine needle aspirates (FNA), or surgical excisions; or biopsy from non-cutaneous tissues such as lymph node tissue, mucosa, conjuctiva, or uvea, other embodiments.
  • the biological sample can be obtained by shaving, waxing, or stripping the region of interest on the skin.
  • a non-limiting example of a product for stripping skin for RNA recovery is the EGIR′ tape strip product (DermTech International, La Jolla, Calif., see also, Wachsman et al., 2011, Brit. J.
  • Representative biopsy techniques include, but are not limited to, excisional biopsy, incisional biopsy, needle biopsy, surgical biopsy.
  • An “excisional biopsy” refers to the removal of an entire tumor mass with a small margin of normal tissue surrounding it.
  • An “incisional biopsy” refers to the removal of a wedge of tissue that includes a cross-sectional diameter of the tumor.
  • a diagnosis or prognosis made by endoscopy or fluoroscopy can require a “core-needle biopsy” of the tumor mass, or a “fine-needle aspiration biopsy” which generally contains a suspension of cells from within the tumor mass.
  • the biological sample may be a microdissected sample, such as a PALM-laser (Carl Zeiss MicroImaging GmbH, Germany) capture microdissected sample.
  • a sample may also be a sample of muscosal surfaces, blood and blood fractions or products (e.g., serum, plasma, platelets, red blood cells, white blood cells, circulating tumor cells isolated from blood, free DNA isolated from blood, and the like), sputum, lymph and tongue tissue, cultured cells, e.g., primary cultures, explants, and transformed cells, stool, urine, etc.
  • the sample may also be vascular tissue or cells from blood vessels such as microdissected blood vessel cells of endothelial origin.
  • a sample is typically obtained from a eukaryotic organism, most preferably a mammal such as a primate e.g., chimpanzee or human; cow; dog; cat; a rodent, e.g., guinea pig; rat; mouse; rabbit.
  • a mammal such as a primate e.g., chimpanzee or human; cow; dog; cat; a rodent, e.g., guinea pig; rat; mouse; rabbit.
  • a sample can be treated with a fixative such as formaldehyde and embedded in paraffin (FFPE) and sectioned for use in the methods of the invention.
  • FFPE formaldehyde and embedded in paraffin
  • fresh or frozen tissue may be used.
  • These cells may be fixed, e.g., in alcoholic solutions such as 100% ethanol or 3:1 methanol:acetic acid.
  • Nuclei can also be extracted from thick sections of paraffin-embedded specimens to reduce truncation artifacts and eliminate extraneous embedded material.
  • biological samples, once obtained, are harvested and processed prior to hybridization using standard methods known in the art. Such processing typically includes protease treatment and additional fixation in an aldehyde solution such as formaldehyde.
  • methylation analysis procedures are known in the art and may be used to practice the invention. These assays allow for determination of the methylation state of one or a plurality of CpG sites within a tissue sample. In addition, these methods may be used for absolute or relative quantification of methylated nucleic acids.
  • Another embodiment of the invention are methods of detecting melanoma based on the differentially methylated sites found in tissue analysis described herein, and not differentially methylated in cultured melanocytes and/or melanoma cell lines. Such methylation assays involve, among other techniques, two major steps.
  • the first step is a methylation specific reaction or separation, such as (i) bisulfite treatment, (ii) methylation specific binding, or (iii) methylation specific restriction enzymes.
  • the second major step involves (i) amplification and detection, or (ii) direct detection, by a variety of methods such as (a) PCR (sequence-specific amplification) such as Taqman(91, (b) DNA sequencing of untreated and bisulfite-treated DNA, (c) sequencing by ligation of dye-modified probes (including cyclic ligation and cleavage), (d) pyrosequencing, (e) single-molecule sequencing, (f) mass spectroscopy, or (g) Southern blot analysis.
  • restriction enzyme digestion of PCR products amplified from bisulfite-converted DNA may be used, e.g., the method described by Sadri & Hornsby (1996 , Nucl. Acids Res. 24:5058-5059), or COBRA (Combined Bisulfite Restriction Analysis) (Xiong & Laird, 1997 , Nucleic Acids Res. 25:2532-2534).
  • COBRA analysis is a quantitative methylation assay useful for determining DNA methylation levels at specific gene loci in small amounts of genomic DNA. Briefly, restriction enzyme digestion is used to reveal methylation-dependent sequence differences in PCR products of sodium bisulfite-treated DNA.
  • Methylation-dependent sequence differences are first introduced into the genomic DNA by standard bisulfite treatment according to the procedure described by Frommer et al. (Frommer et al., 1992 , Proc. Nat. Acad. Sci. USA, 89, 1827-1831). PCR amplification of the bisulfite converted DNA is then performed using primers specific for the CpG sites of interest, followed by restriction endonuclease digestion, gel electrophoresis, and detection using specific, labeled hybridization probes. Methylation levels in the original DNA sample are represented by the relative amounts of digested and undigested PCR product in a linearly quantitative fashion across a wide spectrum of DNA methylation levels.
  • Typical reagents for COBRA analysis may include, but are not limited to: PCR primers for specific gene (or methylation-altered DNA sequence or CpG island); restriction enzyme and appropriate buffer; gene-hybridization oligo; control hybridization oligo; kinase labeling kit for oligo probe; and radioactive nucleotides.
  • bisulfite conversion reagents may include: DNA denaturation buffer; sulfonation buffer; DNA recovery reagents or kits (e.g., precipitation, ultrafiltration, affinity column); desulfonation buffer; and DNA recovery components.
  • MSP Methylation-Specific PCR
  • Methylation-Specific PCR allows for assessing the methylation status of virtually any group of CpG sites within a CpG island, independent of the use of methylation-sensitive restriction enzymes (Herman et al., 1996 , Proc. Nat. Acad. Sci. USA, 93, 9821-9826; U.S. Pat. Nos. 5,786,146, 6,017,704, 6,200,756, 6,265,171 (Herman & Baylin) U.S. Pat. Pub. No. 2010/0144836 (Van Engeland et al.); which are hereby incorporated by reference in their entirety).
  • MSP Methylation-Specific PCR
  • DNA is modified by sodium bisulfite converting unmethylated, but not methylated cytosines to uracil, and subsequently amplified with primers specific for methylated versus unmethylated DNA.
  • MSP requires only small quantities of DNA, is sensitive to 0.1% methylated alleles of a given CpG island locus, and can be performed on DNA extracted from paraffin-embedded samples.
  • Typical reagents e.g., as might be found in a typical MSP-based kit
  • MSP analysis may include, but are not limited to: methylated and unmethylated PCR primers for specific gene (or methylation-altered DNA sequence or CpG island), optimized PCR buffers and deoxynucleotides, and specific probes.
  • the ColoSureTM test is a commercially available test for colon cancer based on the MSP technology and measurement of methylation of the vimentin gene (Itzkowitz et al., 2007, Clin Gastroenterol. Hepatol. 5(1), 111-117).
  • QM-PCR quantitative multiplexed methylation specific PCR
  • the MethyLight and Heavy Methyl assays are a high-throughput quantitative methylation assay that utilizes fluorescence-based real-time PCR (Taq Man®) technology that requires no further manipulations after the PCR step (Eads, C. A. et al., 2000 , Nucleic Acid Res. 28, e 32; Cottrell et al., 2007, J. Urology 177, 1753, U.S. Pat. No. 6,331,393 (Laird et al.), the contents of which are hereby incorporated by reference in their entirety).
  • Taq Man® fluorescence-based real-time PCR
  • the MethyLight process begins with a mixed sample of genomic DNA that is converted, in a sodium bisulfite reaction, to a mixed pool of methylation-dependent sequence differences according to standard procedures (the bisulfite process converts unmethylated cytosine residues to uracil). Fluorescence-based PCR is then performed either in an “unbiased” (with primers that do not overlap known CpG methylation sites) PCR reaction, or in a “biased” (with PCR primers that overlap known CpG dinucleotides) reaction. Sequence discrimination can occur either at the level of the amplification process or at the level of the fluorescence detection process, or both.
  • the MethyLight assay may be used as a quantitative test for methylation patterns in the genomic DNA sample, wherein sequence discrimination occurs at the level of probe hybridization.
  • the PCR reaction provides for unbiased amplification in the presence of a fluorescent probe that overlaps a particular putative methylation site.
  • An unbiased control for the amount of input DNA is provided by a reaction in which neither the primers, nor the probe overlie any CpG dinucleotides.
  • a qualitative test for genomic methylation is achieved by probing of the biased PCR pool with either control oligonucleotides that do not “cover” known methylation sites (a fluorescence-based version of the “MSP” technique), or with oligonucleotides covering potential methylation sites.
  • Typical reagents e.g., as might be found in a typical MethyLight-based kit
  • for MethyLight analysis may include, but are not limited to: PCR primers for specific gene (or methylation-altered DNA sequence or CpG island); TaqMan® probes; optimized PCR buffers and deoxynucleotides; and Taq polymerase.
  • MethyLight technology is used for the commercially available tests for lung cancer (epi proLung BL Reflex Assay); colon cancer (epi proColon assay and mSEPT9 assay) (Epigenomics, Berlin, Germany) PCT Pub. No. WO 2003/064701 (Schweikhardt and Sledziewski), the contents of which is hereby incorporated by reference in its entirety.
  • Quantitative MethyLight uses bisulfite to convert genomic DNA and the methylated sites are amplified using PCR with methylation independent primers. Detection probes specific for the methylated and unmethylated sites with two different fluorophores provides simultaneous quantitative measurement of the methylation.
  • the Heavy Methyl technique begins with bisulfate conversion of DNA. Next specific blockers prevent the amplification of unmethylated DNA. Methylated genomic DNA does not bind the blockers and their sequences will be amplified. The amplified sequences are detected with a methylation specific probe. (Cottrell et al., 2004, Nuc. Acids Res. 32, e10, the contents of which is hereby incorporated by reference in its entirety).
  • the Ms-SNuPE technique is a quantitative method for assessing methylation differences at specific CpG sites based on bisulfite treatment of DNA, followed by single-nucleotide primer extension (Gonzalgo & Jones, 1997 , Nucleic Acids Res. 25, 2529-2531). Briefly, genomic DNA is reacted with sodium bisulfite to convert unmethylated cytosine to uracil while leaving 5-methylcytosine unchanged. Amplification of the desired target sequence is then performed using PCR primers specific for bisulfite-converted DNA, and the resulting product is isolated and used as a template for methylation analysis at the CpG site(s) of interest.
  • Typical reagents for Ms-SNuPE analysis may include, but are not limited to: PCR primers for specific gene (or methylation-altered DNA sequence or CpG island); optimized PCR buffers and deoxynucleotides; gel extraction kit; positive control primers; Ms-SNuPE primers for specific gene; reaction buffer (for the Ms-SNuPE reaction); and radioactive nucleotides.
  • bisulfite conversion reagents may include: DNA denaturation buffer; sulfonation buffer; DNA recovery regents or kit (e.g., precipitation, ultrafiltration, affinity column); desulfonation buffer; and DNA recovery components.
  • MBD-FC methyl binding domain of MBD2
  • MBD-FC Fc fragment of an antibody
  • This fusion protein has several advantages over conventional methylation specific antibodies.
  • the MBD FC has a higher affinity to methylated DNA and it binds double stranded DNA. Most importantly the two proteins differ in the way they bind DNA.
  • Methylation specific antibodies bind DNA stochastically, which means that only a binary answer can be obtained.
  • the methyl binding domain of MBD-FC binds DNA molecules regardless of their methylation status.
  • the strength of this protein—DNA interaction is defined by the level of DNA methylation.
  • eluate solutions of increasing salt concentrations can be used to fractionate non-methylated and methylated DNA allowing for a more controlled separation (Gebhard et al., 2006 , Nucleic Acids Res. 34 e82). Consequently this method, called Methyl-CpG immunoprecipitation (MCIP), not only enriches, but also fractionates genomic DNA according to methylation level, which is particularly helpful when the unmethylated DNA fraction should be investigated as well.
  • MCIP Methyl-CpG immunoprecipitation
  • 5-methyl cytidine antibodies may be used to bind and precipitate methylated DNA.
  • Antibodies are available from Abcam (Cambridge, Mass.), Diagenode (Sparta, N.J.) or Eurogentec (c/o AnaSpec, Fremont, Calif.).
  • MIRA methylated CpG-island recovery assay
  • MeDIP methylated DNA immunoprecipitation
  • methyl-sensitive enzymes that preferentially or substantially cleave or digest at their DNA recognition sequence if it is non-methylated.
  • an unmethylated DNA sample will be cut into smaller fragments than a methylated DNA sample.
  • a hypermethylated DNA sample will not be cleaved.
  • methyl-sensitive enzymes that cleave at their DNA recognition sequence only if it is methylated.
  • Methyl-sensitive enzymes that digest unmethylated DNA suitable for use in methods of the technology include, but are not limited to, Hpall, Hhal, Maell, BstUI and Acil.
  • An enzyme that can be used is Hpall that cuts only the unmethylated sequence CCGG.
  • Another enzyme that can be used is Hhal that cuts only the unmethylated sequence GCGC. Both enzymes are available from New England BioLabs®, Inc. Combinations of two or more methyl-sensitive enzymes that digest only unmethylated DNA can also be used. Suitable enzymes that digest only methylated DNA include, but are not limited to, Dpnl, which only cuts at fully methylated 5′-GATC sequences, and McrBC, an endonuclease, which cuts DNA containing modified cytosines (5-methylcytosine or 5-hydroxymethylcytosine or N4-methylcytosine) and cuts at recognition site 5′ . . . Pu m C(N 40-3000 ) Pu m C . . .
  • the MCA technique is a method that can be used to screen for altered methylation patterns in genomic DNA, and to isolate specific sequences associated with these changes (Toyota et al., 1999, Cancer Res. 59, 2307-2312, U.S. Pat. No. 7,700,324 (Issa et al.) the contents of which are hereby incorporated by reference in their entirety).
  • restriction enzymes with different sensitivities to cytosine methylation in their recognition sites are used to digest genomic DNAs from primary tumors, cell lines, and normal tissues prior to arbitrarily primed PCR amplification. Fragments that show differential methylation are cloned and sequenced after resolving the PCR products on high-resolution polyacrylamide gels.
  • Typical reagents for MCA analysis may include, but are not limited to: PCR primers for arbitrary priming Genomic DNA; PCR buffers and nucleotides, restriction enzymes and appropriate buffers; gene-hybridization oligos or probes; control hybridization oligos or probes.
  • HRM real time PCR machines
  • HRM may also be combined with other amplification techniques such as pyrosequencing as described by Candiloro et al. (Candiloro et al., 2011, Epigenetics 6(4) 500-507). Any of SEQ ID NO 1-353, or portions thereof, may be used in a HRM assay.
  • Another method for analyzing methylation sites is a primer extension assay, including an optimized PCR amplification reaction that produces amplified targets for analysis using mass spectrometry.
  • the assay can also be done in multiplex.
  • Mass spectrometry is a particularly effective method for the detection of polynucleotides associated with the differentially methylated regulatory elements. The presence of the polynucleotide sequence is verified by comparing the mass of the detected signal with the expected mass of the polynucleotide of interest. The relative signal strength, e.g., mass peak on a spectra, for a particular polynucleotide sequence indicates the relative population of a specific allele, thus enabling calculation of the allele ratio directly from the data. This method is described in detail in PCT Pub.
  • WO 2005/012578A1 (Beaulieu et al.) which is hereby incorporated by reference in its entirety.
  • the assay can be adopted to detect bisulfite introduced methylation dependent C to T sequence changes.
  • These methods are particularly useful for performing multiplexed amplification reactions and multiplexed primer extension reactions (e g., multiplexed homogeneous primer mass extension (hME) assays) in a single well to further increase the throughput and reduce the cost per reaction for primer extension reactions.
  • multiplexed amplification reactions and multiplexed primer extension reactions e g., multiplexed homogeneous primer mass extension (hME) assays
  • WO 2006/031745 (Van Der Boom and Boecker); WO 2009/073251 A1(Van Den Boom et al.); WO 2009/114543 A2 (Oeth et al.); and WO 2010/033639 A2 (Ehrich et al.); which are hereby incorporated by reference in their entirety.
  • DNA methylation analysis includes restriction landmark genomic scanning (RLGS, Costello et al., 2002, Meth. Mol. Biol., 200, 53-70), methylation-sensitive-representational difference analysis (MS-RDA, Ushijima and Yamashita, 2009 , Methods Mol Biol. 507, 117-130).
  • RGS restriction landmark genomic scanning
  • MS-RDA methylation-sensitive-representational difference analysis
  • MS-RDA methylation-sensitive-representational difference analysis
  • MS-RDA methylation-sensitive-representational difference analysis
  • Yamashita 2009 , Methods Mol Biol. 507, 117-130.
  • CHARM relative methylation
  • the Roche® NimbleGen® microarrays including the Chromatin Immunoprecipitation-on-chip (ChIP-chip) or methylated DNA immunoprecipitation-on-chip (MeDIP-chip).
  • the nucleic acid may be subjected to sequence-based analysis. Furthermore, once it is determined that one particular melanoma genomic sequence is hypermethylated or hypomethylated compared to the benign counterpart, the amount of this genomic sequence can be determined. Subsequently, this amount can be compared to a standard control value and serve as an indication for the melanoma. In many instances, it is desirable to amplify a nucleic acid sequence using any of several nucleic acid amplification procedures which are well known in the art.
  • nucleic acid amplification is the chemical or enzymatic synthesis of nucleic acid copies which contain a sequence that is complementary to a nucleic acid sequence being amplified (template).
  • the methods and kits of the invention may use any nucleic acid amplification or detection methods known to one skilled in the art, such as those described in U.S. Pat. No. 5,525,462 (Takarada et al.); U.S. Pat. No. 6,114,117 (Hepp et al.); U.S. Pat. No. 6,127,120 (Graham et al.); U.S. Pat. No. 6,344,317 (Urnovitz); U.S. Pat. No. 6,448,001 (Oku); U.S. Pat. No. 6,528,632 (Catanzariti et al.); and PCT Pub. No. WO 2005/111209 (Nakajima et al.); all of which are incorporated herein by reference in their entirety.
  • the nucleic acids are amplified by PCR amplification using methodologies known to one skilled in the art.
  • amplification can be accomplished by any known method, such as ligase chain reaction (LCR), Q ⁇ -replicase amplification, rolling circle amplification, transcription amplification, self-sustained sequence replication, nucleic acid sequence-based amplification (NASBA), each of which provides sufficient amplification.
  • LCR ligase chain reaction
  • Q ⁇ -replicase amplification Q ⁇ -replicase amplification
  • rolling circle amplification transcription amplification
  • self-sustained sequence replication nucleic acid sequence-based amplification
  • NASBA nucleic acid sequence-based amplification
  • Branched-DNA technology may also be used to qualitatively demonstrate the presence of a sequence of the technology, which represents a particular methylation pattern, or to quantitatively determine the amount of this particular genomic sequence in a sample.
  • Nolte reviews branched-DNA signal amplification for direct quantitation of nucle
  • PCR PCR reagents and protocols are also available from commercial vendors, such as Roche Molecular Systems.
  • PCR may be carried out as an automated process with a thermostable enzyme. In this process, the temperature of the reaction mixture is cycled through a denaturing region, a primer annealing region, and an extension reaction region automatically. Machines specifically adapted for this purpose are commercially available.
  • Amplified sequences may also be measured using invasive cleavage reactions such as the Invader® technology (Zou et al., 2010, Association of Clinical Chemistry (AACC) poster presentation on Jul. 28, 2010, “Sensitive Quantification of Methylated Markers with a Novel Methylation Specific Technology,” available at www.exactsciences.com; and U.S. Pat. No. 7,011,944 (Prudent et al.) which are incorporated herein by reference in their entirety).
  • Invader® technology Zaou et al., 2010, Association of Clinical Chemistry (AACC) poster presentation on Jul. 28, 2010, “Sensitive Quantification of Methylated Markers with a Novel Methylation Specific Technology,” available at www.exactsciences.com; and U.S. Pat. No. 7,011,944 (Prudent et al.) which are incorporated herein by reference in their entirety).
  • Suitable next generation sequencing technologies are widely available. Examples include the 454 Life Sciences platform (Roche, Branford, Conn.) (Margulies et al. 2005 Nature, 437, 376-380); Illumina's Genome Analyzer, GoldenGate Methylation Assay, or Infinium Methylation Assays, i.e., Infinium HumanMethylation 27K BeadArray or VeraCode GoldenGate methylation array (Illumina, San Diego, Calif.; Bibkova et al., 2006, Genome Res. 16, 383-393; U.S. Pat. Nos. 6,306,597 and 7,598,035 (Macevicz); U.S. Pat. No.
  • Each of these platforms allow sequencing of clonally expanded or non-amplified single molecules of nucleic acid fragments.
  • Certain platforms involve, for example, (i) sequencing by ligation of dye-modified probes (including cyclic ligation and cleavage), (ii) pyrosequencing, and (iii) single-molecule sequencing.
  • Pyrosequencing is a nucleic acid sequencing method based on sequencing by synthesis, which relies on detection of a pyrophosphate released on nucleotide incorporation.
  • sequencing by synthesis involves synthesizing, one nucleotide at a time, a DNA strand complimentary to the strand whose sequence is being sought.
  • Study nucleic acids may be immobilized to a solid support, hybridized with a sequencing primer, incubated with DNA polymerase, ATP sulfurylase, luciferase, apyrase, adenosine 5′ phosphsulfate and luciferin. Nucleotide solutions are sequentially added and removed.
  • An example of a system that can be used by a person of ordinary skill based on pyrosequencing generally involves the following steps: ligating an adaptor nucleic acid to a study nucleic acid and hybridizing the study nucleic acid to a bead; amplifying a nucleotide sequence in the study nucleic acid in an emulsion; sorting beads using a picoliter multiwell solid support; and sequencing amplified nucleotide sequences by pyrosequencing methodology (e.g., Nakano et al., 2003, J. Biotech. 102, 117-124).
  • Such a system can be used to exponentially amplify amplification products generated by a process described herein, e.g., by ligating a heterologous nucleic acid to the first amplification product generated by a process described herein.
  • Certain single-molecule sequencing embodiments are based on the principal of sequencing by synthesis, and utilize single-pair Fluorescence Resonance Energy Transfer (single pair FRET) as a mechanism by which photons are emitted as a result of successful nucleotide incorporation.
  • the emitted photons often are detected using intensified or high sensitivity cooled charge-couple-devices in conjunction with total internal reflection microscopy (TIRM). Photons are only emitted when the introduced reaction solution contains the correct nucleotide for incorporation into the growing nucleic acid chain that is synthesized as a result of the sequencing process.
  • TIRM total internal reflection microscopy
  • FRET FRET based single-molecule sequencing or detection
  • energy is transferred between two fluorescent dyes, sometimes polymethine cyanine dyes Cy3 and Cy5, through long-range dipole interactions.
  • the donor is excited at its specific excitation wavelength and the excited state energy is transferred, non-radiatively to the acceptor dye, which in turn becomes excited.
  • the acceptor dye eventually returns to the ground state by radiative emission of a photon.
  • the two dyes used in the energy transfer process represent the “single pair”, in single pair FRET. Cy3 often is used as the donor fluorophore and often is incorporated as the first labeled nucleotide.
  • Cy5 often is used as the acceptor fluorophore and is used as the nucleotide label for successive nucleotide additions after incorporation of a first Cy3 labeled nucleotide.
  • the fluorophores generally are within 10 nanometers of each other for energy transfer to occur successfully.
  • Bailey et al. recently reported a highly sensitive (15 pg methylated DNA) method using quantum dots to detect methylation status using fluorescence resonance energy transfer (MS-qFRET)(Bailey et al. 2009, Genome Res. 19(8), 1455-1461, which is incorporated herein by reference in its entirety).
  • An example of a system that can be used based on single-molecule sequencing generally involves hybridizing a primer to a study nucleic acid to generate a complex; associating the complex with a solid phase; iteratively extending the primer by a nucleotide tagged with a fluorescent molecule; and capturing an image of fluorescence resonance energy transfer signals after each iteration (e.g., Braslaysky et al., PNAS 100(7): 3960-3964 (2003); U.S. Pat. No. 7,297,518 (Quake et al.) which are incorporated herein by reference in their entirety).
  • Such a system can be used to directly sequence amplification products generated by processes described herein.
  • the released linear amplification product can be hybridized to a primer that contains sequences complementary to immobilized capture sequences present on a solid support, a bead or glass slide for example.
  • Hybridization of the primer-released linear amplification product complexes with the immobilized capture sequences immobilizes released linear amplification products to solid supports for single pair FRET based sequencing by synthesis.
  • the primer often is fluorescent, so that an initial reference image of the surface of the slide with immobilized nucleic acids can be generated. The initial reference image is useful for determining locations at which true nucleotide incorporation is occurring. Fluorescence signals detected in array locations not initially identified in the “primer only” reference image are discarded as non-specific fluorescence.
  • the bound nucleic acids often are sequenced in parallel by the iterative steps of, a) polymerase extension in the presence of one fluorescently labeled nucleotide, b) detection of fluorescence using appropriate microscopy, TIRM for example, c) removal of fluorescent nucleotide, and d) return to step a with a different fluorescently labeled nucleotide.
  • Digital PCR was developed by Kalinina and colleagues (Kalinina et al., 1997 , Nucleic Acids Res. 25; 1999-2004) and further developed by Vogelstein and Kinzler (1999 , Proc. Natl. Acad. Sci. U.S.A. 96; 9236-9241).
  • the application of digital PCR is described by Cantor et al. (PCT Pub. Nos. WO 2005/023091A2 (Cantor et al.); WO 2007/092473 A2, (Quake et al.)), which are hereby incorporated by reference in their entirety.
  • Digital PCR takes advantage of nucleic acid (DNA, cDNA or RNA) amplification on a single molecule level, and offers a highly sensitive method for quantifying low copy number nucleic acid.
  • Fluidigm® Corporation offers systems for the digital analysis of nucleic acids.
  • nucleotide sequencing may be by solid phase single nucleotide sequencing methods and processes.
  • Solid phase single nucleotide sequencing methods involve contacting sample nucleic acid and solid support under conditions in which a single molecule of sample nucleic acid hybridizes to a single molecule of a solid support. Such conditions can include providing the solid support molecules and a single molecule of sample nucleic acid in a “microreactor.” Such conditions also can include providing a mixture in which the sample nucleic acid molecule can hybridize to solid phase nucleic acid on the solid support.
  • Single nucleotide sequencing methods useful in the embodiments described herein are described in PCT Pub. No. WO 2009/091934 (Cantor).
  • nanopore sequencing detection methods include (a) contacting a nucleic acid for sequencing (“base nucleic acid,” e.g., linked probe molecule) with sequence-specific detectors, under conditions in which the detectors specifically hybridize to substantially complementary subsequences of the base nucleic acid; (b) detecting signals from the detectors and (c) determining the sequence of the base nucleic acid according to the signals detected.
  • the detectors hybridized to the base nucleic acid are disassociated from the base nucleic acid (e.g., sequentially dissociated) when the detectors interfere with a nanopore structure as the base nucleic acid passes through a pore, and the detectors disassociated from the base sequence are detected.
  • a detector also may include one or more regions of nucleotides that do not hybridize to the base nucleic acid.
  • a detector is a molecular beacon.
  • a detector often comprises one or more detectable labels independently selected from those described herein. Each detectable label can be detected by any convenient detection process capable of detecting a signal generated by each label (e.g., magnetic, electric, chemical, optical and the like). For example, a CD camera can be used to detect signals from one or more distinguishable quantum dots linked to a detector.
  • the invention encompasses any method known in the art for enhancing the sensitivity of the detectable signal in such assays, including, but not limited to, the use of cyclic probe technology (Bakkaoui et al., 1996, BioTechniques 20: 240-8, which is incorporated herein by reference in its entirety); and the use of branched probes (Urdea et al., 1993, Clin. Chem. 39, 725-6; which is incorporated herein by reference in its entirety).
  • the hybridization complexes are detected according to well-known techniques in the art.
  • Reverse transcribed or amplified nucleic acids may be modified nucleic acids.
  • Modified nucleic acids can include nucleotide analogs, and in certain embodiments include a detectable label and/or a capture agent.
  • detectable labels include, without limitation, fluorophores, radioisotopes, colorimetric agents, light emitting agents, chemiluminescent agents, light scattering agents, enzymes and the like.
  • capture agents include, without limitation, an agent from a binding pair selected from antibody/antigen, antibody/antibody, antibody/antibody fragment, antibody/antibody receptor, antibody/protein A or protein G, hapten/anti-hapten, biotin/avidin, biotin/streptavidin, folic acid/folate binding protein, vitamin B 12/intrinsic factor, chemical reactive group/complementary chemical reactive group (e.g., sulfhydryl/maleimide, sulfhydryl/haloacetyl derivative, amine/isotriocyanate, amine/succinimidyl ester, and amine/sulfonyl halides) pairs, and the like.
  • Modified nucleic acids having a capture agent can be immobilized to a solid support in certain embodiments.
  • the invention may encompass detecting and/or quantitating using antibodies either alone or in conjunction with measurement of methylation levels.
  • Antibodies are already used in current practice in the classification and/or diagnosis of melanocytic lesions (Alonso et al., 2004 , Am. J. Pathol. 164(1) 193-203; Ivan & Prieto, 2010, Future Oncol. 6(7), 1163-1175; Linos et al., 2011, Biomarkers Med. 5(3) 333-360; and Rothberg et al., 2009 J. Nat. Canc. Inst. 101(7) 452-474, the contents of which are hereby incorporated by reference in their entireties).
  • antibodies examples include HMB45/gp100 (Abcam; AbD Serotec; BioGenex, San Ramon, Calif.; Biocare Medical, Concord, Calif.); MART-1/Melan-A (Abcam; AbD Serotec; BioGenex; Thermo Scientific Pierce Abs., Rockford, Ill.); Microphthalmia transcription factor/MITF-1 (Invitrogen); NKI/C3 (Melanoma Associated Antigen 100+/7 kDa)(Abcam; Thermo Scientific Pierce Abs.); p75NTR/neurotrophin receptor (Abcam; AbD Serotec; Promega, Madison, Wis.); S100 (Abcam; AbD Serotec, Raleigh, N.C.; BioGenex); Tyrosinase (Abcam; AbD Serotec; Thermo Scientific Pierce Abs.).
  • a cocktail of 5100, HMB-45 and MART-1/Melan-A is used.
  • Antibodies may also be used to detect the gene products of the methylated genes described herein. Specifically, genes hypomethylated would be expected to show over-expression and genes hypermethylated would be expected to show under-expression. Staining markers of tumor vascular formation may also be used in conjunction with the present invention (Bhati et al., 2008 , Am. J. Pathol. 172(5), 1381-1390, including Table 1 on page 1387, the contents of which are incorporated herein by reference in their entirety).
  • Antibody reagents can be used in assays to detect expression levels of in patient samples using any of a number of immunoassays known to those skilled in the art. Immunoassay techniques and protocols are generally described in Price and Newman, “ Principles and Practice of Immunoassay ,” 2nd Edition, Grove's Dictionaries, 1997; and Gosling, “ Immunoassays: A Practical Approach ,” Oxford University Press, 2000. A variety of immunoassay techniques, including competitive and non-competitive immunoassays, can be used. See, e.g., Self et al., 1996, Curr. Opin. Biotechnol., 7, 60-65.
  • immunoassay encompasses techniques including, without limitation, enzyme immunoassays (EIA) such as enzyme multiplied immunoassay technique (EMIT), enzyme-linked immunosorbent assay (ELISA), IgM antibody capture ELISA (MAC ELISA), and microparticle enzyme immunoassay (MEIA); capillary electrophoresis immunoassays (CEIA); radioimmunoassays (RIA); immunoradiometric assays (IRMA); fluorescence polarization immunoassays (FPIA); and chemiluminescence assays (CL). If desired, such immunoassays can be automated. Immunoassays can also be used in conjunction with laser induced fluorescence.
  • EIA enzyme multiplied immunoassay technique
  • ELISA enzyme-linked immunosorbent assay
  • MAC ELISA IgM antibody capture ELISA
  • MEIA microparticle enzyme immunoassay
  • CEIA capillary electrophoresis immunoassay
  • Liposome immunoassays such as flow-injection liposome immunoassays and liposome immunosensors, are also suitable for use in the present invention. See, e.g., Rongen et al., 1997 , J. Immunol. Methods, 204, 105-133.
  • nephelometry assays in which the formation of protein/antibody complexes results in increased light scatter that is converted to a peak rate signal as a function of the marker concentration, are suitable for use in the methods of the present invention.
  • Nephelometry assays are commercially available from Beckman Coulter (Brea, Calif.) and can be performed using a Behring Nephelometer Analyzer (Fink et al., 1989, J. Clin. Chem. Clin. Biochem., 27, 261-276).
  • Direct labels include fluorescent or luminescent tags, metals, dyes, radionuclides, and the like, attached to the antibody.
  • An antibody labeled with iodine—125 125 I can be used.
  • a chemiluminescence assay using a chemiluminescent antibody specific for the nucleic acid is suitable for sensitive, non-radioactive detection of protein levels.
  • An antibody labeled with fluorochrome is also suitable.
  • fluorochromes examples include, without limitation, DAPI, fluorescein, Hoechst 33258, R-phycocyanin, B-phycoerythrin, R-phycoerythrin, rhodamine, Texas red, and lissamine.
  • Indirect labels include various enzymes well known in the art, such as horseradish peroxidase (HRP), alkaline phosphatase (AP), ⁇ -galactosidase, urease, and the like.
  • HRP horseradish peroxidase
  • AP alkaline phosphatase
  • AP alkaline phosphatase
  • ⁇ -galactosidase urease
  • a horseradish-peroxidase detection system can be used, for example, with the chromogenic substrate tetramethylbenzidine (TMB), which yields a soluble product in the presence of hydrogen peroxide that is detectable at 450 nm.
  • An alkaline phosphatase detection system can be used with the chromogenic substrate p-nitrophenyl phosphate, for example, which yields a soluble product readily detectable at 405 nm.
  • a ⁇ -galactosidase detection system can be used with the chromogenic substrate o-nitrophenyl- ⁇ -D-galactopyranoside (ONPG), which yields a soluble product detectable at 410 nm
  • An urease detection system can be used with a substrate such as urea-bromocresol purple (Sigma Immunochemicals; St. Louis, Mo.).
  • a signal from the direct or indirect label can be analyzed, for example, using a spectrophotometer to detect color from a chromogenic substrate; a radiation counter to detect radiation such as a gamma counter for detection of 125 I; or a fluorometer to detect fluorescence in the presence of light of a certain wavelength.
  • a quantitative analysis can be made using a spectrophotometer such as an EMAX Microplate Reader (Molecular Devices; Menlo Park, Calif.) in accordance with the manufacturer's instructions.
  • the assays of the present invention can be automated or performed robotically, and the signal from multiple samples can be detected simultaneously.
  • the antibodies can be immobilized onto a variety of solid supports, such as magnetic or chromatographic matrix particles, the surface of an assay plate (e.g., microtiter wells), pieces of a solid substrate material or membrane (e.g., plastic, nylon, paper), and the like.
  • An assay strip can be prepared by coating the antibody or a plurality of antibodies in an array on a solid support. This strip can then be dipped into the test sample and processed quickly through washes and detection steps to generate a measurable signal, such as a colored spot.
  • the antibodies may be in an array one or more antibodies, single or double stranded nucleic acids, proteins, peptides or fragments thereof, amino acid probes, or phage display libraries.
  • FISH Fluorescence in situ Hybridization
  • CGH Comparative Genomic Hybridization
  • the invention may further encompass detecting and/or quantitating using fluorescence in situ hybridization (FISH) in a sample, preferably a tissue sample, obtained from a subject in accordance with the methods of the invention.
  • FISH fluorescence in situ hybridization
  • a sample preferably a tissue sample
  • FISH fluorescence in situ hybridization
  • CGH comparative genomic hybridization
  • the invention encompasses use of additional melanoma specific gene expression and/or antibody assays either in situ, i.e., directly upon tissue sections (fixed and/or frozen) of patient tissue obtained from biopsies or resections, such that no nucleic acid purification is necessary; or based on extracted and/or amplified nucleic acids.
  • Targets for such assays are disclosed in Haqq et al. 2005 , Proc. Nat. Acad. Sci. USA, 102(17), 6092-6097; Riker et al., 2008, BMC Med. Genomics, 1, 13, pub. 28 Apr. 2008; Hoek et al., 2004, Can. Res. 64, 5270-5282; PCT Pub. Nos.
  • WO 2008/030986 and WO 2009/111661 Kashani-Sabet & Haqq); U.S. Pat. No. 7,247,426 (Yakhini et al.), all of which are incorporated herein by reference in their entirety.
  • miRNA microRNAs
  • These methods could be used in combination with the methylation methods described herein (see Mueller et al., 2009 , J. Invest. Dermatol., 129, 1740-1751; Leidinger et al., 2010, BMC Cancer, 10, 262; U.S. Pat. Pub. 2009/0220969 (Chiang and Shi); PCT Pub. No.
  • methylated nucleic acids may be detected in blood either as free DNA or in circulating tumor cells.
  • in situ procedures see, e.g., Nuovo, G. J., 1992, PCR In Situ Hybridization: Protocols And Applications , Raven Press, NY, which is incorporated herein by reference in its entirety.
  • nucleic acid microarrays Methods for making nucleic acid microarrays are known to the skilled artisan and are described, for example, in Lockhart et al., 1996, Nat. Biotech. 14,1675-1680, 1996 Schena et al., 1996 , Proc. Natl. Acad. Sci. USA, 93, 10614-10619, U.S. Pat. No. 5,837,832 (Chee et al.) and PCT Pub. No. WO 00/56934 (Englert et al.), herein incorporated by reference.
  • oligonucleotides may be synthesized or bound to the surface of a substrate using a chemical coupling procedure and an ink jet application apparatus, as described U.S. Pat. No. 6,015,880 (Baldeschweiler et al.), incorporated herein by reference.
  • a gridded array may be used to arrange and link cDNA fragments or oligonucleotides to the surface of a substrate using a vacuum system, thermal, UV, mechanical or chemical bonding procedure.
  • the measurement of differentially methylated elements associated with melanoma may alone, or in conjunction with other melanoma detection tools discussed above (antibody staining, PCR, CGH, FISH) may have several other non-limiting uses. Amongst these uses are: (i) reclassifying specimens that were indeterminate or difficult to identify in a pathology laboratory; (ii) deciding to follow up with a lymph node examination and/or PET/CAT/MRI or other imaging methods; (iii) determining the frequency of follow up visits; or (iv) initiating other investigatory analysis such as a blood draw and evaluation for circulating tumor cells. Furthermore, the differentially methylated elements associated with melanoma may help to determine which patients would benefit from adjuvant treatment after surgical resection.
  • the invention provides compositions and kits measuring methylation or polypeptides or polynucleotides regulated by the differentially methylated elements described herein using DNA methylation specific assays, antibodies specific for the polypeptides or nucleic acids specific for the polynucleotides.
  • Kits for carrying out the diagnostic assays of the invention typically include, in suitable container means, (i) a reagent for methylation specific reaction or separation, (ii) a probe that comprises an antibody or nucleic acid sequence that specifically binds to the marker polypeptides or polynucleotides of the invention, (iii) a label for detecting the presence of the probe and (iv) instructions for how to measure the level of methylation (or polypeptide or polynucleotide).
  • kits may include several antibodies or polynucleotide sequences encoding polypeptides of the invention, e.g., a first antibody and/or second and/or third and/or additional antibodies that recognize a protein encoded by a gene differentially methylated in melanoma.
  • the container means of the kits will generally include at least one vial, test tube, flask, bottle, syringe and/or other container into which a first antibody specific for one of the polypeptides or a first nucleic acid specific for one of the polynucleotides of the present invention may be placed and/or suitably aliquoted.
  • kits of the present invention will also typically contain means for containing the antibody or nucleic acid probes in close confinement for commercial sale.
  • Such containers may include injection and/or blow-molded plastic containers into which the desired vials are retained.
  • kits may further comprise positive and negative controls, as well as instructions for the use of kit components contained therein, in accordance with the methods of the present invention.
  • the various markers of the invention also provide reagents for in vivo imaging such as, for instance, the imaging of metastasis of melanoma to regional lymph nodes using labeled reagents that detect (i) DNA methylation associated with melanoma, (ii) a polypeptide or polynucleotide regulated by the differentially methylated elements.
  • In vivo imaging techniques may be used, for example, as guides for surgical resection or to detect the distant spread of melanoma.
  • reagents that detect the presence of these proteins or genes, such as antibodies may be labeled with a positron-emitting isotope (e.g., 18 F) for positron emission tomography (PET), gamma-ray isotope (e.g., 99mTc) for single photon emission computed tomography (SPECT), a paramagnetic molecule or nanoparticle (e.g., Gd 3+ chelate or coated magnetite nanoparticle) for magnetic resonance imaging (MRI), a near-infrared fluorophore for near-infra red (near-IR) imaging, a luciferase (firefly, bacterial, or coelenterate), green fluorescent protein, or other luminescent molecule for bioluminescence imaging, or a perfluorocarbon-filled vesicle for ultrasound.
  • FDG Fluorodeoxyglucose
  • such reagents may include a fluorescent moiety, such as a fluorescent protein, peptide, or fluorescent dye molecule.
  • fluorescent dyes include, but are not limited to, xanthenes such as rhodamines, rhodols and fluoresceins, and their derivatives; bimanes; coumarins and their derivatives such as umbelliferone and aminomethyl coumarins; aromatic amines such as dansyl; squarate dyes; benzofurans; fluorescent cyanines; carbazoles; dicyanomethylene pyranes, polymethine, oxabenzanthrane, xanthene, pyrylium, carbostyl, perylene, acridone, quinacridone, rubrene, anthracene, coronene, phenanthrecene, pyrene, butadiene, stilbene, lanthanide metal chelate complexes, rare-earth metal chelate
  • Fluorescent dyes are discussed, for example, in U.S. Pat. No. 4,452,720 (Harada et al.); U.S. Pat. No. 5,227,487 (Haugland and Whitaker); and U.S. Pat. No. 5,543,295 (Bronstein et al.).
  • Other fluorescent labels suitable for use in the practice of this invention include a fluorescein dye.
  • Typical fluorescein dyes include, but are not limited to, 5-carboxyfluorescein, fluorescein-5-isothiocyanate and 6-carboxyfluorescein; examples of other fluorescein dyes can be found, for example, in U.S. Pat. No.
  • kits may include a rhodamine dye, such as, for example, tetramethylrhodamine-6-isothiocyanate, 5-carboxytetramethylrhodamine, 5-carboxy rhodol derivatives, tetramethyl and tetraethyl rhodamine, diphenyldimethyl and diphenyldiethyl rhodamine, dinaphthyl rhodamine, rhodamine 101 sulfonyl chloride (sold under the tradename of TEXAS RED®, and other rhodamine dyes.
  • a rhodamine dye such as, for example, tetramethylrhodamine-6-isothiocyanate, 5-carboxytetramethylrhodamine, 5-carboxy rhodol derivatives, tetramethyl and tetraethyl rhodamine, diphen
  • kits may include a cyanine dye, such as, for example, Cy3, Cy3B, Cy3.5, Cy5, Cy5.5, Cy7.
  • Phosphorescent compounds including porphyrins, phthalocyanines, polyaromatic compounds such as pyrenes, anthracenes and acenaphthenes, and so forth, may also be used.
  • a variety of methods may be used to identify compounds that modulate DNA methylation and prevent or treat melanoma progression.
  • an assay that provides a readily measured parameter is adapted to be performed in the wells of multi-well plates in order to facilitate the screening of members of a library of test compounds as described herein.
  • an appropriate number of cells can be plated into the cells of a multi-well plate, and the effect of a test compound on the expression of a gene differentially methylated in melanoma can be determined.
  • the compounds to be tested can be any small chemical compound, or a macromolecule, such as a protein, sugar, nucleic acid or lipid.
  • test compounds will be small chemical molecules and peptides.
  • any chemical compound can be used as a test compound in this aspect of the invention, although most often compounds that can be dissolved in aqueous or organic (especially DMSO-based) solutions are used.
  • the assays are designed to screen large chemical libraries by automating the assay steps and providing compounds from any convenient source to assays, which are typically run in parallel (e.g., in microtiter formats on microtiter plates in robotic assays). It will be appreciated that there are many suppliers of chemical compounds, including Sigma (St. Louis, Mo.), Aldrich (St. Louis, Mo.), Sigma-Aldrich (St. Louis, Mo.), Fluka Chemika-Biochemica Analytika (Buchs Switzerland) and the like.
  • high throughput screening methods involve providing a combinatorial chemical or peptide library containing a large number of potential therapeutic compounds.
  • Such “combinatorial chemical libraries” or “ligand libraries” are then screened in one or more assays, as described herein, to identify those library members (particular chemical species or subclasses) that display a desired characteristic activity. In this instance, such compounds are screened for their ability to modulate the expression of gene differentially methylated in melanoma.
  • a combinatorial chemical library is a collection of diverse chemical compounds generated by either chemical synthesis or biological synthesis, by combining a number of chemical “building blocks” such as reagents.
  • a linear combinatorial chemical library such as a polypeptide library is formed by combining a set of chemical building blocks (amino acids) in every possible way for a given compound length (i.e., the number of amino acids in a polypeptide compound). Millions of chemical compounds can be synthesized through such combinatorial mixing of chemical building blocks.
  • combinatorial chemical libraries include, but are not limited to, peptide libraries (see, e.g., U.S. Pat. No. 5,010,175 (Rutter and Santi), Furka, 1991, Int. J. Pept. Prot. Res., 37:487-493; and Houghton et al., 1991, Nature, 354:84-88).
  • Other chemistries for generating chemical diversity libraries can also be used. Such chemistries include, but are not limited to: U.S. Pat. No. 6,075,121 (Bartlett et al.) peptoids; U.S. Pat. No.
  • Biotech., 14(3):309-314 carbohydrate libraries, e.g., Liang et al., 1996, Science, 274:1520-1522, small organic molecule libraries (see, e.g., benzodiazepines, Baum, 1993, C&EN, January 18, page 33.
  • Devices for the preparation of combinatorial libraries are commercially available (see, e.g., 357 MPS, 390 MPS, Advanced Chem Tech, Louisville Ky., Symphony, Rainin, Woburn, Mass., 433 A Applied Biosystems, Foster City, Calif., 9050 Plus, Millipore, Bedford, Mass.).
  • Methylation modifiers are known and have been the basis for several approved drugs.
  • Major classes of enzymes are DNA methyl transferases (DNMTs), histone deacetylases (HDACs), histone methyl transferases (HMTs), and histone acetylases (HATs).
  • DNMT inhibitors azacitidine (Vidaza®) and decitabine have been approved for myelodysplastic syndromes (for a review see Musolino et al., 2010, Eur. J. Haematol. 84, 463-473; Issa, 2010, Hematol. Oncol. Clin. North Am.
  • HDAC inhibitor has been approved by FDA for treating cutaneous T-cell lymphoma (CTCL) for patients with progressive, persistent, or recurrent disease (Marks and Breslow, 2007, Nat. Biotech. 25(1), 84-90).
  • compound libraries include: DNA methyl transferase (DNMT) inhibitor libraries available from Chem Div (San Diego, Calif.); cyclic peptides (Nauman et al., 2008, ChemBioChem 9, 194-197); natural product DNMT libraries (Medina-Franco et al, 2010, Mol. Divers., Springer, published online 10 Aug. 2010); HDAC inhibitors from a cyclic a33-tetrapeptide library (Olsen and Ghadiri, 2009, J. Med. Chem. 52(23), 7836-7846); HDAC inhibitors from chlamydocin (Nishino et al., 2006, Amer. Peptide Symp. 9(7), 393-394).
  • DNMT DNA methyl transferase
  • nucleic acids such as antisense nucleic acids, siRNAs or ribozymes
  • Ribozymes that cleave mRNA at site-specific recognition sequences can be used to destroy target mRNAs, particularly through the use of hammerhead ribozymes.
  • Hammerhead ribozymes cleave mRNAs at locations dictated by flanking regions that form complementary base pairs with the target mRNA.
  • the target mRNA has the following sequence of two bases: 5′-UG-3′.
  • the construction and production of hammerhead ribozymes is well known in the art.
  • FFPE paraffin-embedded
  • the UNC melanoma database manager extracted demographic and clinical information from the medical chart, including age, sex, anatomic sites of nevi and melanomas, and Breslow depth and Clark level of melanomas.
  • H&E hematoxylin and eosin
  • the Mel-505 melanoma and MCF-7 breast tumor cell lines were used to establish assay conditions and to assess assay reproducibility and the effects of formalin-fixation and contamination by non-melanocytic cells on methylation profiles.
  • Cell lines were grown in RPMI medium with 10% fetal bovine serum and harvested while in log growth phase. Cells were pelleted and divided into two portions. One portion was used for DNA extraction (non-fixed) and the other pellet was fixed in buffered formalin, embedded in paraffin, and sections were cut from the paraffin blocks and were mounted on uncoated glass slides.
  • FFPE normal skin tissue was obtained from breast reduction specimens under IRB approval.
  • DNA was prepared from formalin-fixed nevi, melanoma, or normal skin tissues, or cell line pellets as previously published (Thomas et al., 2007, Cancer Epidemiol Biomarkers Prev. 16, 991-977). DNA was purified from non-fixed cell lines or peripheral blood leukocytes using the FlexiGene DNA according to the manufacturer's instructions (Qiagen, Valencia, Calif.). 6.3. Bisulfite Treatment of DNA
  • EZ DNA Methylation Gold kit Zymo Research, Orange, Calif.
  • Approximately 500-1000 ng DNA from each tissue specimen was mixed with 130 ⁇ l of CT Conversion Reagent in a PCR tube and cycled in a thermal cycler at 98° C. for 10 minutes, 64° C. for 2.5 hours, and stored at 4° C. for up to 20 hours.
  • the sample was then mixed with 600 ⁇ l M-binding buffer and spun through the Zymo-Spin IC column for 30 seconds ( ⁇ 10,000 ⁇ g).
  • the column was washed with 100 ⁇ l of M-Wash buffer, spun, and incubated in 200 ⁇ l of M-Desulphonation buffer for 15-20 minutes. The column was then spun for 30 seconds (at ⁇ 10,000 ⁇ g), washed twice with 200 ul M-Wash buffer, and spun at top speed. The sample was eluted from the column with 10 ⁇ l M-Elution buffer and stored in a ⁇ 20° C. freezer prior to use in the Illumina GoldenGate Methylation assay. After bisulfite treatment, DNA quantity and concentration were measured by a Nanodrop spectrophotometer, and DNA concentration adjusted to 50-60 ng/ ⁇ l.
  • Array-based DNA methylation profiling was accomplished using the Illumina GoldenGate Cancer Panel I methylation bead array (Illumina, San Diego, Calif.) to simultaneously interrogate 1505 CpG loci associated with 807 cancer-related genes. Bead arrays were run in the Mammalian Genotyping Core laboratory at the University of North Carolina. The Illumina GoldenGate methylation assay was performed as described previously (Bibikova et al., 2006, Genome Res., 16, 383-393). Two allele-specific oligonucleotides (ASO) and 1 locus-specific oligo (LSO) are designed to interrogate each CpG site, with the LSO containing a sequence which corresponds to a specific address on the BeadArray.
  • ASO allele-specific oligonucleotides
  • LSO 1 locus-specific oligo
  • Bisulfite-converted DNAs were biotinylated and bound to paramagnetic particles, hybridized to ASO and LSO probes, and the hybridized ASO oligos were extended in a methylation-specific fashion, then ligated to the LSO probe to create amplifiable templates.
  • the joining of two fragments to create a PCR template provides an added level of locus specificity.
  • the PCR that followed used 2 fluorescently-labeled (Cy3, Cy5) and biotinylated universal PCR primers corresponding to the ASO sequences (P1, P2) and a common P3 primer that binds to the LSO sequence.
  • Controls for methylation status used on each bead array included the Zymo Universal Methylated DNA Standard as the positive, fully-methylated control, and a GenomePlex (Sigma) whole genome amplified (WGA) DNA used as the negative, unmethylated control.
  • the data were assembled using the GenomeStudio Methylation software from Illumina (San Diego, Calif.). All array data points were represented by fluorescent signals from both methylated (Cy5) and unmethylated (Cy3) alleles. Background intensity computed from the negative control was subtracted from each data point.
  • the BeadStudio Methylation Module software (Illumina) was used to create scatter plots to examine the relationship between cell line replicates and between FFPE and non-fixed samples. The correlation coefficient, R 2 , was calculated for each comparison.
  • a detection p-value computed by GenomeStudio and representing the probability that the signal from a given CpG locus is distinguishable from the negative controls was used as a metric for quality control for sample performance.
  • ⁇ values with a detection p-value greater than 10 ⁇ 5 were considered unreliable and set to be missing (Marsit et al, 2009, Carcinogenesis, 30, 416-422).
  • Two nevus samples with more than 25% missing ⁇ values and 39 CpG loci with more than 20% missing samples were excluded from analysis.
  • the final data contained 988 CpG loci in 646 genes and 49 samples (22 melanomas and 27 moles).
  • AUC receiver operating characteristics curve
  • the DAVID Bioinformatics Resources 6.7 Functional Annotation Tool http://david.abcc.ncifcrf.gov/home.jsp was used to perform gene-GO term enrichment analysis to identify the most relevant GO terms associated with the genes found to be differentially methylated between nevi and malignant melanomas. Gene function was also investigated using GeneCards (http://www.genecards.org/).
  • FIGS. 1A-1C are replicate methylation array profiles of non-formalin-fixed MCF-7 breast tumor cell DNA, formalin-fixed DNA from the Mel-505 melanoma cell line, as well as methylation profiles from non-fixed versus FFPE Mel-505 DNA. Each of these array replicates produced was highly reproducible, showing r 2 values of ⁇ 0.98.
  • the Mel-505 cell line DNA was diluted with increasing proportions (from 0 to 50%) of DNA from normal peripheral blood leukocytes (PBLs) (90% Mel-505/10% PBL, 80% Mel-505/20% PBL, 70% Mel-505/30% PBL, 60% Mel-505/40% PBL, 50% Mel-505/50% PBL), and each mixture was plotted against the profile for pure (100%) Mel-505 cell line DNA.
  • PBLs peripheral blood leukocytes
  • This result provides a guideline for estimating the necessary purity of tumor DNA to achieve methylation array results that are representative of melanocytic target DNA.
  • Illumina methylation array analysis was performed on 27 FFPE benign nevi, 22 FFPE primary malignant melanomas and 9 FFPE lymph node metastatic melanomas.
  • the patient characteristics as well as histologic and clinical features of these tissues are detailed in Table 1 below.
  • the mean age of nevus patients (29 years) was significantly less than melanoma patients (61 years; p ⁇ 0.0001).
  • melanoma patients 61 years; p ⁇ 0.0001
  • 83% were younger than 40 yrs
  • only 27% of melanoma patients were younger than 40 yrs.
  • Forty-one percent of nevus patients and 50% of melanoma patients were male.
  • HN head and neck
  • melanomas occurring mostly on either the trunk (36%) or an extremity (41%).
  • nevi 38% were classified histologically as intradermal melanocytic nevi, 31% were described as compound melanocytic nevi, and 21% were identified as compound melanocytic nevi with congenital pattern. Only 7% of nevi were classified as being compound dysplastic nevi with slight atypia.
  • melanomas 50% were of the superficial spreading histologic type, 14% were lentigo maligna, 14% were acral lentiginous, 9% were nodular, and 9% were spindle cell melanoma.
  • the melanomas consisted mostly of deeper lesions, with 32% having a Breslow depth of ⁇ 1.5 mm, and 68% having Breslow depth of >1.5
  • Illumina GoldenGate Cancer Panel I methylation profiling to evaluate promoter methylation patterns in 27 benign nevi and 22 primary melanomas.
  • Illumina methylation array results were subjected to filtering to remove 68 probes that corresponded to CpG sites on the X chromosome and 410 probes that were reported to contain a SNP or repeat (Byun et al, 2009), thus making them unreliable in some samples.
  • ⁇ values with a detection p-value greater than 10 ⁇ 5 were considered unreliable and set as missing data points (Marsit et al, 2009); using this criterium, two nevus samples with more than 25% missing 13 values as well as 39 CpG loci with ⁇ values missing in more than 20% missing samples were excluded from analysis.
  • the final data set consisted of 988 CpG loci within 646 genes in 49 specimens (22 melanomas and 27 moles).
  • Unsupervised hierarchical clustering was used to compare methylation patterns at 988 CpG loci in benign nevi and malignant melanomas. Clustering produced a clear separation of melanomas from benign nevi, with two major clusters of nevi and at least four clusters of melanomas identified, suggesting that the methylation signature of melanomas is fundamentally distinct from that of nevi.
  • class comparison analyses 75 CpG sites in 63 genes were identified that differed significantly (with P values of ⁇ 0.05) between nevi and melanomas after Bonferroni correction for multiple comparisons; a list of these 75 loci is provided in Table 2.
  • the loci that significantly distinguished melanomas from nevi based on methylation were KCNK4, GSTM2, TRIP6 (2 sites), FRZB, COL1A2, NPR2, which showed hypermethylation, and CARD15/NOD2, KLK10, MPO, EVI2A, EMR3 (2 sites), HLA-DPA1, PTHR1, IL2, TNFSF8, LAT, PSCA, IFNG, PTHLH, three sites in RUNX3 (3 sites), ITK, CD2, OSM (2 sites), and CCL3, which showed hypomethylation in melanomas compared with nevi.
  • Prediction Analysis for Microarray was carried out to assess the classification of melanoma and nevus samples by the method of nearest shrunken centroids.
  • the PAM algorithm automatically identifies CpG loci that contribute most to the melanoma classification.
  • the optimal shrinkage threshold was chosen to be 4.28 with 12 CpG loci required for optimal classification. This approach yielded a zero cross-validation error, with no misclassification.
  • the 12 CpG loci identified by PAM analysis that provided the most accurate prediction of melanoma were: RUNX3_P393_R, RUNX3_P247_F, RUNX3_E27_R, COL1A2_E299_F, MPO_P883_R, TNFSF8_E258_R, CD2_P68_F, EVI2A_P94_R, OSM_P168_F, ITK_P114_F, FRZB_P406_F, ITK_E166_R. All but one locus (ITK_E166_R) exhibited mean ⁇ differences between melanomas and nevi of ⁇ 0.2.
  • the box plots shown in FIGS. 3A-3L display the mean, range, and standard deviation of ⁇ values in nevi and melanomas for the 12 CpG sites that are highly predictive of melanoma as determined by PAM analysis. For most CpG loci showing hypomethylation in melanomas compared with benign nevi, mean methylation ⁇ values were very high (nearly 1.0), indicating that these CpG sites were uniformly highly methylated in nevi, however, methylation was lost to varying degrees in primary melanomas.
  • FRZB_P406_F and COL1A2_E299_F were poorly methylated in nevi, having mean ⁇ values near 0.1, but showed considerably higher methylation in many melanomas, with mean ⁇ values between 0.6 and 0.7.
  • FIGS. 4A-4O which plot the sensitivity versus the specificity of the 12 CpG loci identified by PAM analysis.
  • the area under the curve (AUC) ranged from 0.89 to 0.90 for the 2 hypermethylated loci, and from 0.96 to 1.00 for the 10 hypomethylated loci.
  • two of the RUNX3 probes (RUNX3_P247_F and RUNX3_P393_R) exhibited both 100% sensitivity and 100% specificity in identifying melanomas.
  • Data on sequences showing differences in methylation levels ( ⁇ values) may be found in Table 6 for a combined analysis where metastases were included with melanomas.
  • Descriptions of sequences, methylation sites from the Illumina array and gene names may be found in Table 4A and 4B for the melanoma vs. benign nevi comparison.
  • Data for the metastases vs. benign nevi comparison may be found in Table 5A and 5B (Section 6.10).
  • Some additional specific sequences methylated in the metastatic samples may be found in Tables 7A and 7B.
  • Specific sequences and methylation sites for other CpG probes may be obtained from the gene list for the Illumina GoldenGate Cancer Panel 1.
  • Table 3B provides gene functional information obtained through gene ontology searches using the DAVID Bioinformatics Resources 6.7 (http://david.abcc.ncifcrf.gov/home.jsp) and the human gene database, GeneCards (http://www.genecards.org). Details on the mean ⁇ in nevi and melanomas, mean ⁇ differences, adjusted p-values, and AUC (and the sensitivity and specificity of melanoma prediction) for each gene are presented in Table 3A.
  • T-cell signaling and/or natural killer cell cytotoxicity IFNG, IL2, ITK, LAT, CD2, CCL3, TNFSF8, HLA-DPA1
  • EMR3 myeloid-myeloid cell interactions
  • MPO neutrophil microbicidal activity
  • CARD15/NOD2 neutrophil microbicidal activity
  • TRIP6 NF- ⁇ B activation
  • RUNX3, FRZB, TNFSF8, KLK10, PSCA, OSM, COL1A2 genes have well-characterized roles in cancer cell growth, cell adhesion, or apoptosis.
  • the 3 CpG sites located within the RUNX3 gene all exhibited significantly lower methylation in melanomas compared with nevi even though RUNX3 has been considered a tumor suppressor gene and might be expected to display promoter hypermethylation, rather than hypomethylation, in malignancy (Kitago et al., 2009, Clin. Cancer Res. 15, 2988-2994).
  • RUNX3 may have both tumor suppressor and oncogenic functions depending on the cellular context (Chuang and Ito, 2010, Oncogene 29, 2605-2615).
  • TK_E166_R mean methylation ⁇ value differences between nevi and melanomas of ⁇ 0.2. All loci except ITK_E166_R exhibited. Probes were ranked by significance (adjusted P value) within each of the hypermethylated and hypomethylated groups. P value, nevus mean ⁇ , and melanoma mean ⁇ were each adjusted for age, sex, multiple comparisons using Bonferroni correction. AUC; area under the ROC curve. Methylation status in normal skin and peripheral blood leukocytes (U; unmethylated ( ⁇ 0.0-0.3), PM; partially methylated ( ⁇ 0.3-0.7), M; highly methylated ( ⁇ 0.8-1.0)).
  • Table 4A shows the accession numbers; specific single CpG coordinate; presence or absence of CpG islands; specific sequences used in the Illumina GoldenGate array experiments; and the synonyms for the genes hypomethylated in melanoma. All Accession numbers and location are based on Ref. Seq. version 36.1.
  • Table 4B shows the accession numbers; specific single CpG coordinate; presence or absence of CpG islands; specific sequences used in the Illumina GoldenGate array experiments; and the synonyms for the genes hypermethylated in melanoma. All Accession numbers and location are based on Ref. Seq. version 36.1.
  • the methylation data for nine melanoma metastases was compared with the benign moles. Eighteen more Genes/CpG sites were found to be significant in this comparison with nine additional hypomethylated and nine hypermethylated genes.
  • the metastases sample descriptions may be found in Table 1. For results of metastases vs. benign nevi see Table 5A and 5B below. For results of combined melanomas and metastases vs. benign nevi see Table 6A and 6B below. For gene descriptions and methylated sequences of the 18 significant additional genes see Table 7A and Table 7B.
  • Table 5A shows the methylation sites, methylation levels, ⁇ values for benign nevi and metastatic melanomas and difference in ⁇ values for genes hypermethylated in melanoma metastasis.
  • Table 7A shows the accession numbers; specific single CpG coordinate; presence or absence of CpG islands; specific sequences used in the Illumina GoldenGate array experiments; and the synonyms for additional genes hypomethylated in melanoma metastasis. All Accession numbers and location are based on Ref. Seq. version 36.1.
  • Table 7B shows the accession numbers; specific single CpG coordinate; presence or absence of CpG islands; specific sequences used in the Illumina GoldenGate array experiments; and the synonyms for additional genes hypermethylated in melanoma metastasis. All Accession numbers and location are based on Ref. Seq. version 36.1.
  • sample set #2 an independent set of 25 melanomas and 29 nevi underwent DNA methylation profiling using the Illumina GoldenGate Cancer Panel I and passed filtering criteria.
  • the melanomas were of a variety of histologic subtypes and ranged in Breslow thickness from 0.42 to 10.75 mm.
  • the majority of nevi 21 of 29 had varying degree of histologic atypia.
  • 14 were also statistically significant for differential methylation in an independent data set including dysplastic nevi after adjustment for age, sex and multiple comparisons.
  • the 14 genes were CARD15, CD2, EMR3 (2 CpG loci), EVI2A, FRZB, HLA-DPA1, IFNG, IL2, ITK, LAT, MPO, PTHLH, RUNX3 (3 CpG loci), and TNFSF8.
  • FRZB_E186 CpG locus rather than FRZB_P406 was significantly differentially methylated in sample set #2.
  • the AUC's for CpG sites within these genes remained high in sample set #2, ranging from 0.79 to 0.97. See Conway et al., 2011, Pigment Cell Melanoma Res. 24 352-360, and supplemental materials, the contents of which are hereby incorporated by reference.
  • Illumina methylation array results were subjected to filtering using the same criterion as in the earlier sets of nevi and melanoma.
  • Initial results found 91 CpG sites hypermethylated and 72 CpG sites hypomethylated in metastases when compared to nevi.
  • FIG. 5 shows a Venn diagram of CpG sites that statistically significantly distinguish between nevi (dysplastic and non-dysplastic) and primary melanomas or metastases.
  • the number of statistically significant differential CpG sites, after Bonferoni correction for multiple comparisons and adjusting for age and gender, (p ⁇ 0.05) are listed for each of the three comparisons.
  • 58 CpG sites distinguish between nevi and melanomas.
  • 75 CpG sites distinguish between nevi and metastases.
  • methylation profiles may be used as a surrogate for measuring the biological characteristic, e.g., Breslow depth, when the location does not lend itself to such measurement, failure to annotate the sample, drug or treatment selection; selection of an appropriate combination of independent and additive conventional diagnostic markers to be used in conjunction with the methylation markers described in this application; or other reasons.
  • Table 10 lists CpG methylation sites associated with Breslow depth.
  • analysis to study mitotic rate (Table 11) and ulceration were performed.
  • one methylation correlated significantly, ProbeID MAP3K1_P7_F with a p value of 0.00096.
  • the results for Breslow depth, mitotic rate, and mutations are shown below.
  • ProbeID p.value.Mut.Uni q.value.Mut.Uni p.value.Mut.Multi q.value.Mut.Multi CCR5_P630_R 0.05511171 0.492144064 0.000689708 0.16766822 CD40_E58_R 0.001758825 0.273985791 0.000717553 0.16766822 DNMT3B_P352_R 0.001006177 0.230434732 0.000641606 0.16766822 GPX1_P194_F 0.001592276 0.273985791 0.000201973 0.16766822 KLK10_P268_R 6.22E ⁇ 05 0.0872197 0.000400032 0.16766822 P2RX7_E323_R 0.001008864 0.230434732 0.000663112 0.16766822 SEMA3B_P110_R 0.001328043 0.267401202 0.000895024 0.240377935 Table ⁇ shows
  • HsaIIIB cg14703690 GNG7_E310_R FLJ00058 cg13502721 HOXA9_E252_R HOX1, ABD-B, HOX1G, HOX1.7, MGC1934 cg10604830 HOXA9_P303_F HOX1, ABD-B, HOX1G, HOX1.7, MGC1934 cg03715906 IRAK3_P185_F IRAK-M cg24003063 KLK10_P268_R NES1, PRSSL1 cg06130787 MAP3K1_P7_F .
  • Sodium bisulfite modification and methylation-specific PCR (Method A): Digested DNA (500 ng) is denatured in 0.3 N NaOH at 37° C. for 15 min (Clark et al., 1994 , Nucleic Acids Res. 22, 2990-2997). Then, 3.6 N sodium bisulfite (pH 5.0) and 0.6 mM hydroquinone are added, and the sample undergoes 15 cycles of 1) denaturation at 95° C. for 30 s and 2) incubation at 50° C. for 15 min. The sample is desalted with the Wizard DNA Clean-Up system (Promega, Madison, Wis.), and desulfonated in 0.3 N NaOH.
  • MSP Methylation-specific PCR
  • Primers and probes are designed based on the sequences shown in Table 4.
  • the Zymo Universal Methylated DNA Standard is used as the positive, fully-methylated control, and a GenomePlex (Sigma) whole genome amplified (WGA) DNA is used as the negative, unmethylated control.
  • DNA is sodium bisulfite treated using the EZ DNA Methylation-Gold Kit (Zymo Research, cat. #D5005).
  • the DNA sample ( ⁇ 10-20 ul lysate or 200-500 ng DNA) is mixed with 130 ul of CT Conversion Reagent in a PCR tube and denatured in a thermal cycler at 98° C. for 10 minutes, sodium bisulfite modified at 64° C. for 2.5 hours, and stored at 4° C. for up to 20 hours.
  • the column is washed with 100 ul of M-Wash buffer, spun, and incubated in 200 ul of M-Desulphonation buffer for 15-20 minutes.
  • cDNA is synthesized from 3 ng of total RNA using Superscript II (Invitrogen).
  • Real-time PCR is performed using SYBR Green PCR Core Reagents (PE Applied Biosystems, Foster City, Calif.) and an iCycler Thermal Cycler (Bio-Rad Laboratories, Hercules, Calif.). Quantitative RT-PCR is also performed using TaqMan probes and instrumentation (Applied Biosystems, Carlsbad, Calif.).
  • the number of molecules of a specific cDNA in a sample is measured by comparing its amplification with that of standard samples containing 10 1 to 10 6 molecules.
  • the expression levels in each sample are obtained by normalizing the number of its cDNA molecules with that of the GAPDH, actin, or other housekeeping genes.
  • Sodium-bisulfite modified DNA is PCR amplified in a final volume of 20 uL PCR buffer containing 10 mM Tris-HCl (pH8.3), 50 mM KCl, 2.5-4.5 mM MgCl2, 150-250 nM dNTPs, 0.2-0.4 uM primers, and 0.5 Units of AmpliTaq Gold polymerase (ABI) for an initial denaturation at 95° C. for 10 minutes followed by 45 cycles at 95° C.-15s, 55-66° C.-30s, 72° C.-30s, and a final extension at 72° C. for 7 minutes.
  • AmpliTaq Gold polymerase AmpliTaq Gold polymerase
  • Controls used to quantify methylation values include serially diluted methylated/unmethylated DNAs (Zymo) from 100% methylated to 0% methylated for each gene/CpG of interest, no-template control, reference gene (beta-actin) and standard curve of DNA quantity. Reactions are run using SYBR green (Roche) or methylation specific fluorescently labeled probes (ABI) on the ABI 7900HT Fast instrument with software to calculate standard curves and Ct values. Multiplex PCR can be evaluated in the same well for comparison when using fluorescently labeled methylated (FAM) and unmethylated (VIC) TaqMan (ABI) probes using the ABI 7900HT Fast instrument.
  • FAM fluorescently labeled methylated
  • VIC unmethylated
  • ABSI methylated TaqMan
  • Target CpG Islands and Primers for Bisulfite sequencing or MS-HRM and Reference Primers SEQ ID Nos. 340-346 (sense), SEQ ID Nos. 347-353 (antisense).
  • Target ID Sense (5′-3′) Antisense (5′-3′) ITK_P114_F TGAGTTTATAGTTTTTTAAATATTATTTTA TACTCAAAAACAACTTACCTTCAAC ITK_E166_R TGTGTTAAGAGGTGATGTTTAAGGT AACAAATAAAACTACTCACATACCCC ITK_E166_R ATTAAGAAATTTTAATAAAAGAGAA TAAAACTACTCACATACCCCATAAC KIT_P405F-P367R TTTATTGTTTGGGGAGTATTTGGTAGGT CCACCTTTCCACCCCTAAAATATAAAC KLK10_P268_R GGAGATTGTAATAAATTAAGGTTAAAAGAG TAAAACACACACAAAACTCACTCAC MPO_P883_R
  • ITK Immunofluorescence Staining for ITK (IL-2 inducible T-cell kinase).
  • IHC immunohistochemistry
  • the melanoma stained pink for ITK, while the surrounding normal skin does not stain for ITK. No other ITK staining was detected in the surrounding tissue and ITK staining was not detected in the normal melanocytes.
  • the section was stained with an antibody to ITK (abcam; 1:3000) with tyramide Cy5 amplification to visualize ITK (pink color).
  • the specimen was also stained with the blue fluorescent stain DAPI (4′,6-diamidino-2-phenylindole) that binds strongly to A-T rich regions in DNA.
  • DAPI blue fluorescent stain
  • MART1 IHC staining One of current markers for margin control, used primarily when melanomas are removed by MOHs surgery, is MART1 IHC staining. Alternatively, surgeons remove tissue based on an arbitrary distance from the tumor. MART1 is also expressed normal melanocytes so MART1 IHC staining shows the density and distribution of the melanocytes as an indicator of a clear margin. However, ITK IHC staining is present and then abruptly becomes absent at the edge of the tumor. ITK shows melanoma cells migrating along the basement membrane out from the tumor must be removed. ITK staining looks like it could be a better measure of clear margins.
  • the ITK levels for three other melanomas and three nevi were studied quantitatively using Dual Fluorescent Immunohistochemistry and Automated Quantitative Analysis (AQUA) technology. Only melanocytic cells were quantitated using an S100 mask that defines the melanocytic region.
  • Bond Autostainer Leica Microsystems Inc., Norwell Mass.
  • Slides were deparaffinized in Bond dewax solution (AR9222) and hydrated in Bond wash solution (AR9590).
  • Antigen retrieval for ITK and 5100 was performed for 30 min at 1000 C in Bond-epitope retrieval solution 2 pH9.0 (AR9640).
  • H&E stained whole tissue sections were digitally imaged (20 ⁇ objective) using the Aperio ScanScope XT (Aperio Technologies, Vista, Calif.).
  • Aperio Fl. (Aperio Inc) with integrated HistoRx AQUA technology (HistoRx, New Haven, Conn.) was used to scan the whole slides at ⁇ 20 objective through DAPI, CY3 and CY5 channels to identify nuclei, 5100 (mask) and ITK (target proteins) respectively.
  • 5100 positive areas within the tumor were annotated for each slide manually using positive pan tool; out of the focus or folded tissue areas were marked by negative pan to exclude from analysis.
  • Annotated layers for each slide were submitted for analysis through spectrum software (Aperio Inc.) using AQUA clustering algorithm according to AQUAnalysisTM user guide: Aperio Edition (Rev. 1.0, CDN0044, HistoRx, New Haven, Conn.).
  • Generated AQUA analysis data (summary of the AQUA scores and compartment masking produced by AQUA) was pushed back to spectrum and exported as csv file.
  • This application contains a sequence listing. It has been submitted electronically via EFS-Web as an ASCII text file entitled “UNC10001WO-Sequence — Listing_ST25.txt”. The sequence listing is 68 kilobytes in size, and was created on Sep. 12, 2011. It is hereby incorporated by reference in its entirety.

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Abstract

This invention is directed to a method for detecting melanoma in a tissue sample by measuring a level of methylation of one or more regulatory elements differentially methylated in melanoma and benign nevi. The invention provides methods for detecting melanoma, related kits, and methods of screening for compounds to prevent or treat melanoma.

Description

    RELATED APPLICATION
  • This application claims the benefit of U.S. Provisional Patent Application No. 61/382,623, filed Sep. 14, 2010 entitled “Methods and Kits for Detecting Melanoma” naming Nancy Thomas et al. as inventors with Attorney Docket No. UNC10001USV. The entire contents of which are hereby incorporated by reference including all text, tables, and drawings.
    • STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT
  • This invention was made at least in part with government support under grant number 1R21 CA134368-01 awarded by the National Cancer Institute. The United States Government has certain rights in the invention.
    • 1. FIELD OF THE INVENTION
  • This invention relates generally to the discovery of novel differentially methylated regulatory elements associated with melanoma. The invention provides methods for detecting melanoma, related kits, and methods of screening for compounds to prevent or treat melanoma.
    • 2. BACKGROUND OF THE INVENTION 2.1. Skin Cancer and Melanoma
  • Skin cancer is the most common form of cancer. There are two major types of skin cancer, keratinocyte cancers (basal and squamous cell carcinomas) and melanoma. Though melanoma is less than five percent of the skin cancers, it is the seventh most common malignancy in the U.S. and is responsible for most of the skin cancer related deaths. Specifically, the American Cancer Society estimates that in the U.S. 114,000 new cases of melanoma, including 68,000 invasive and 46,000 noninvasive melanomas, will be diagnosed in 2010 and almost 9,000 people will die of melanoma (Jemal et al., CA Cancer J. Clin. 2010 July 7 [Epub ahead of print]). The WHO estimates that 48,000 people die worldwide of melanoma every year (Lucas, R., Global Burden of Disease of Solar Ultraviolet Radiation, Environmental Burden of Disease Series, Jul. 25, 2006; No. 13. News release, World Health Organization).
  • As with many cancers, the clinical outcome for melanoma depends on the stage at the time of the initial diagnosis. When melanoma is diagnosed early, the prognosis is good. However, if diagnosed in late stages, it is a deadly disease. In particular in 2010 the ACS reports that the 5-year survival rate is 92% for melanoma diagnosed when small and localized, stage IA or IB. However, when the melanoma has spread beyond the original area of skin and nearby lymph nodes, the 5-year survival rate drops to 15-20% for distant metastatic disease, or stage IV melanoma. It is therefore imperative to diagnose melanoma in its earliest form. In addition, interventions for melanoma such as use of cytotoxic chemotherapy and other available agents, rarely impact the course of disease (Avril et al., 2004, J. Clin. Oncol. 15, 1118-1125; Middleton et al., 2000, J. Clin. Oncol. 18, 158-166).
    • 2.2. Issues with Melanoma Diagnosis
  • Early diagnosis is difficult due to the overlap in clinical and histopathological features of early melanomas and benign nevi, especially benign atypical nevi (Strauss et al., 2007, Br. J. Dermatol. 157, 758-764). Moreover, there is a sizeable disagreement amongst pathologists regarding the diagnosis of melanoma and benign diseases such as compound melanocytic nevi or Spitz nevi. One study reported a 15% discordance (Shoo et al. 2010, J. Am. Acad. Dermatol. 62(5), 751-756). An earlier study of over 1000 melanocytic lesions reported that an expert panel found a 14% rate of false positives, misclassifying benign lesions as invasive melanoma; and a 17% rate of false negatives, misclassifying malignant melanoma as benign (Veenhuizen et al. 1997, J. Pathol. 182, 266-272). In one study where an expert panel interpreted lesions as melanoma, a group of general pathologists mistakenly diagnosed dysplastic nevi in 12% of the readings (Brochez et al., 2002, J. Pathol. 196, 459-466). In fact, many nevi, especially atypical or dysplastic nevi, are difficult to distinguish from melanoma, even by expert pathologists (Farmer et al., 1996, Hum. Pathol. 27, 528-531). This results in a quandary for clinicians who not only biopsy but re-excise with margins large numbers of benign atypical nevi in the population (Fung, 2003, Arch. Dermatol. 139, 1374-1375), at least, in part, due to lack of confidence in the histopathologic diagnosis. The numbers involved are substantial in the U.S. alone. One study estimated that with 1,500,000 to 4,500,000 annual biopsies of melanocytic neoplasms, 200,000 to 650,000 discordant cases would result annually (Shoo et al. 2010, J. Am. Acad. Dermatol. 62(5), 751-756). This high rate of misdiagnosis is problematic on many levels. The false positives lead to unnecessary costly medical interventions, e.g., overly large excisions, high-dose interleukin-2 or interferon alpha, and needless stress for the patients. The false negatives mean increased likelihood of a presentation with more severe disease, which as discussed above, dramatically increases the risk of a poor clinical outcome and risk of death.
  • Furthermore, current guidelines recommend wide excisional biopsy with 0.5 to 2.0 cm margins for patients presenting with primary melanoma (NCCN, Clin. Pract. Guidelines in Oncology—v.2.2010: Melanoma, Mar. 17, 2010, page ME-B). However, excisional biopsy with such broad margins may not be appropriate for sites such as the face, ears, fingers, palms, or soles of the feet. Better histopathology will improve the ability for doctors to choose the appropriate intervention, such as margin controlled surgery (Mohs surgery) with 0.2 cm margins.
    • 2.3. Standard of Care for Melanoma
  • For suspicious pigmented lesions current guidelines recommend excisional biopsy with 1-3 mm margins and rebiopsy if the sample is inadequate for diagnosis or microstaging. Pathologists typically assess Breslow's depth or thickness, ulceration, mitotic rate, margin status and Clark's level (based on the skin layer penetrated). A positive diagnosis for melanoma may lead to an evaluation for potential spread to the lymph nodes or other organs. Patients with stage I or II melanoma are further staged with sentinel lymph node (SLN) biopsy including immunohistochemical (IHC) staining. IHC is often used as an adjunct to the standard histopathologic examination (hematoxylin and eosin (H&E) staining, etc.) for melanocytic lesions or to determine the tumor of origin. Antibodies such as 5100, HMB-45, Ki-67 (MIB1), MITF and MART-1/Melan-A or cocktails of several may be used for staining (Ivan & Prieto, 2010, Future Oncol. 6(7), 1163-1175; Linos et al., 2011, Biomarkers Med. 5(3) 333-360). In a literature review Rothberg et al. report that melanoma cell adhesion molecule (MCAM)/MUC18, matrix metalloproteinase-2, Ki-67, proliferating cell nuclear antigen (PCNA) and p16/INK4A are predictive of either all-cause mortality or melanoma specific mortality (Rothberg et al., 2009 J. Nat. Canc. Inst. 101(7) 452-474). Rothberg et al. also note that these and other “molecular prognostic markers have largely failed to be incorporated into guidelines, staging systems, or the standard of care for melanoma patients.”
  • Follow up may include cross sectional imaging (CT, MRI, PET). For patients suspected with stage III disease, with clinically positive lymph nodes, guidelines recommend fine needle aspiration or open biopsy of the enlarged lymph node. For patients with distant metastases, stage IV, serum lactate dehydrogenase (LDH) may have a prognostic role (NCCN Guidelines).
  • As discussed above, wide excision is recommended for primary melanoma. For patients with lymph node involvement, stage III, complete lymph dissection may be indicated. For patients with resected stage JIB or III melanoma, some studies have shown that adjuvant interferon alfa has led to longer disease free survival. For first- or second-line stage III and IV melanoma systemic treatments include: carboplatin, cisplatin, dacarbazine, interferon alfa, high-dose interleukin-2, paclitaxel, temozolomide, vinblastine or combinations thereof (NCCN Guidelines, ME-D, MS-9-13). Recently, the FDA approved Zelboraf™ (vemurafenib, also known as INN, PLX4032, RG7204 or R05185426) for unresectable or metastatic melanoma with the BRAF V600E mutation (Bollag et al., 2010, Nature 467, 596-599, Chapman et al., 2011, New Eng. J. Med. 364 2507-2516). Another recently approved drug for unresectable or metastatic melanoma is Yervoy® (ipilimumab) an antibody which binds to cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) (Hodi et al., 2010, New Eng. J. Med. 363 711-723). Others recently reported that patients with KIT receptor activating mutations or over-expression responded to Gleevac® (imatinib mesylate) (Carvajal et al., 2011, JAMA 305(22) 2327-2334).
    • 2.4. Emerging Molecular Diagnostic Tools
  • Ivan and Prieto review recent reports of antibodies associated with melanoma pathogenesis but their prognostic significance is unclear. Specifically, they discuss work with adhesion molecules (catenins, claudins), apoptosis inhibitors (survivin), cell cycle regulators (cyclins, HDM2, Ki67), growth factors and receptors (c-Kit/SCF, KIT, VEGF, VEGF R3), signaling molecules (Akt), transcription factors (ATF-1), and tumor suppressors (p53, PTEN). Others have reported use of a tissue microarray to predict melanoma progression and in particular found that Ki67, p16INK4a, p21CIP1 and Bcl-6 correlated with metastatic disease (Alonso et al., 2004, Am. J. Pathol. 164(1) 193-203).
  • In a study of melanoma progression, Haqq et al. show gene expression patterns associated with metastatic melanomas (Haqq et al., 2005, Proc. Nat. Acad. Sci. USA, 102(17), 6092-6097). The value of these markers is uncertain because the researchers used a very small sample set melanoma (N=6) and moles (N=9). Riker et al. report gene expression profiles of primary and metastatic melanomas (Riker et al., 2008, BMC Med. Genomics, 1, 13, pub. 28 Apr. 2008). Limited numbers of frozen melanomas and nevi have been profiled using 19K-41K gene expression arrays (Haqq et al., 2005; Scatolini et al., 2010, Int. J. Cancer 126:1869-81; Talantov et al., 2005, Clin. Cancer Res. 11:7234-42). Upon further investigation of candidate markers on an FFPE training set, Kashani-Sabet et al. achieved a 91% sensitivity and 95% specificity using a 5-marker IHC panel analyzed with a composite diagnostic algorithm that takes into account the distribution of staining from top-to-bottom of the specimen (Kashani-Sabet et al., 2009, Proc. Nat. Acad. Sci. USA, 106:6268-72). Alexandrescu et al. found that, using RT-PCR for unequivocal melanoma vs. benign nevi, candidate markers SILV, GDF15, and L1CAM normalized to TYR gave areas under the curve (AUC) of 0.94, 0.67, and 0.5, respectively, while SILV, the best marker, gave an AUC of 0.74 for differentiating melanoma from atypical nevi (Alexandrescu et al., 2010, J. Invest. Dermatol. 130:1887-92). In a different study, candidate gene expression differences were selected for FFPE primary cutaneous melanomas (N=38) vs. conventional nevi (N=48) using a custom gene expression array probing 1,100 unique genes (Koh et al., 2009, Mod. Pathol. 22:538-46). A leave-one-out′ cross-validation using a 100 probe qPCR-based classifier incorporating candidate markers showed concordance of 89% between gene classification and histopathologic diagnosis for all samples (N=120 melanomas and nevi) (Koh et al., 2009).
  • Others have studied both proteins and nucleic acids associated with melanocytes transforming into melanomas (Hoek et al., 2004, Can. Res. 64, 5270-5282). Bastian et al. describe comparative genomic hybridization (CGH) as a means to find patterns of chromosomal aberrations associated with melanoma (Bastian et al., 2003, Am. J. Pathol. 163(5), 1765-1770). The utility of CGH in a clinical setting is limited because it currently requires approximately a microgram of DNA and about a month for results. Gerami et al. report a fluorescence in situ hybridization (FISH) panel of 4 probes, chromosome 6p25, 6 centromere, 6q23 and 11qβ showed a 86.7% sensitivity and 95.4% specificity (Gerami et al., 2009, Am. J. Surg. Pathol. 33(8) 1146-1156). FISH for melanoma has shown promise in the clinic and healthcare providers currently reimburse such tests. However, FISH is better for detecting amplifications than deletions so some information from CGH is lost.
  • Recent studies show that activating mutations in the BRAF or NRAS oncogenes occur in approximately 50% (Thomas et al., 2004, J. Invest Dermatol. 122, 1245-1250; Edlundh-Rose et al., 2006, Melanoma Res. 16, 471-478; Thomas et al., 2007, Cancer Epidemiol. Biomarkers Prev. 16, 991-977) and 20% (Edlundh-Rose et al., 2006; Thomas et al., 2007) of primary cutaneous melanomas, respectively. However, the majority of nevi also contain these mutations (Pollock et al., 2003, Nat. Genet. 33, 19-20; reviewed in Thomas et al., 2006, Melanoma Res. 16, 97-103, Uribe et al. 2006, Am. J. Dermatopathol. 25, 365-370; Poynter et al., 2006, Melanoma Res. 16, 267-273; Wu et al., 2007, J. Dermatopathol. 29, 534-537), which limits their usefulness for melanoma diagnosis. As mentioned above, Zelboraf™ (vemurafenib) has been approved for patients with the BRAF V600E mutation. As a companion diagnostic, the FDA approved the Roche Cobas® 4800 V600 BRAF Mutation Test for use on formalin-fixed paraffin-embedded (FFPE) samples.
  • DNA methylation may provide a tool, in conjunction with histopathology, for the molecular diagnostics of melanoma. DNA methylation is an epigenetic chemical modification that does not alter the sequence code, but can be heritable, and is involved in the regulation of gene expression (Plass, 2002, Hum. Mol. Genet. 11, 2479-2488). The most common methylation site in mammals is a cytosine located next to a guanosine (CpG). Clusters of CpGs, referred to as islands, are found in the 5′ regulatory and promoter regions of genes (Antequera and Bird, 1993, Proc. Natl. Acad. Sci. USA, 90, 11995-11999). Hypermethylation of CpG islands in promoter regions is a common mechanism of tumor suppressor gene silencing in cancer (Balmain et al., 2003, Nat. Genet. 33 Suppl, 238-244; Baylin and Herman, 2000, Trends Genet. 16, 168-174; Feinberg and Tycko, 2004, Nat. Rev. Cancer 4, 143-153; Plass, 2002). Aberrant promoter methylation with silencing of tumor suppressor genes has been shown to occur widely in human melanomas (Furuta et al., 2004, Cancer Sci. 95, 962-968; Hoon et al., 2004, Oncogene 23, 4014-4022; Bonazzi et al., 2008, Genes Chromosomes Cancer, 48, 10-21), and in histologically pre-malignant lesions associated with a variety of cancer types (Fackler et al., 2003, Int. J. Cancer, 107, 970-975). These studies suggest methylation may be useful as an early diagnostic marker for melanoma. However much of the work to date has been performed with passaged cells or cell lines rather than actual tissue samples. Changes associated with passaging and/or immortalization create artifacts that reduce their usefulness (Staveren et al., 2009, Biochim. Biophys. Acta Rev. Cancer, 1795 (2) 92-103).
  • Molecular diagnosis of melanoma holds promise but, due to the small size of melanocytic lesions which are typically submitted in entirety for diagnosis, any new diagnostic tests need to be valid and reproducible in FFPE tissues. Previously, gene expression arrays were used to identify markers of melanoma heterogeneity using cell lines and a few frozen and FFPE melanomas, but found that only 24% of unselected FFPE samples produced RNA of sufficient quality for microarray analysis (Penland et al., 2007, Lab. Invest. 87, 383-391). Improvements in melanoma diagnosis could be accelerated by the use of molecular assays that are less sensitive to tissue fixation than RNA-based assays. Moreover, there is an unmet medical need for improved melanoma diagnosis. The invention described herein provides a solution.
    • 3. SUMMARY OF THE INVENTION
  • In particular non-limiting embodiments, the present invention provides a method for detecting melanoma in a tissue sample which comprises: (a) measuring a level of methylation of one or more regulatory elements differentially methylated in melanoma and benign nevi; and (b) determining whether melanoma is present or absent in the tissue sample. The methylation may be measured at single CpG site resolution. The tissue sample may be a common nevi, a dysplastic nevi, or a benign atypical nevi sample, or a melanocytic lesion of unknown potential. The sample may be prepared in a variety of ways including, but not limited to, a formalin-fixed, paraffin-embedded (FFPE) sample, a fresh-frozen sample, or a fresh tissue sample. There are many sources for the samples, including but not limited to, dissected tissue, an excision biopsy, a needle biopsy, a punch biopsy, a shave biopsy, a tape biopsy, or a skin biopsy. Alternatively, the sample may be from a lymph node biopsy, a sentinel lymph node, or a cancer metastasis.
  • In particular non-limiting embodiments, the present invention provides that the differentially methylatated regulatory elements are elements associated with immune response/inflammatory pathway genes, hormonal regulation genes, or cell growth/cell adhesion/apoptosis genes. The regulatory elements may be associated with a gene encoding CARD15, CCL3, CD2, EMR3, EVI2A, FRZB, GSTM2, HLA-DPA1, IFNG, ITK, KCNK4, KLK10, LAT, MPO, NPR2, OSM, PSCA, PTHLH, PTHR1, RUNX3, TNFSF8 or TRIP6. In one non-limiting embodiment, hypermethylation of the regulatory elements associated with a gene encoding FRZB, GSTM2, KCNK4, NPR2, or TRIP6 is indicative of melanoma. In another non-limiting embodiment, hypomethylation of the regulatory elements associated with a gene encoding CARD15, CCL3, CD2, EMR3, EVI2A, HLA-DPA1, IFNG, ITK, KLK10, LAT, MPO, OSM, PSCA, PTHLH, PTHR1, RUNX3 or TNFSF8 is indicative of melanoma. In one non-limiting embodiment, a panel of 22 genes is used. In another non-limiting embodiment a panel of 14 genes is used. The level of methylation may be measured using a variety of methods including, but not limited to, assays based on bisulfate conversion-based microarray, differential hybridization, methylated DNA immunoprecipitation, methylated CpG island recovery (MIRA), methylation specific polymerase chain reaction (MSP), or methylation-sensitive high resolution melting (MS-HRM). The detection of the differentially methylated elements may also be by microarray or mass spectrometry. The differentially methylated elements may be amplified by pyrosequencing, invasive cleavage amplification, sequencing by ligation, or emulsion-based PCR.
  • In non-limiting embodiments, the regulatory element differentially methylated has a sensitivity analysis area under the curve of greater than 0.70, 0.75, 0.8, 0.85, 0.9, 0.95, 0.98, or 0.99. The levels of methylation for 4 or more regulatory elements may be measured. Alternatively, 8 or 12 or more regulatory elements are measured.
  • In non-limiting embodiments, the method further comprises evaluating the quality of the sample by measuring the levels of skin specific markers using antibody staining, differential methylation, expression analysis, or fluorescence in situ hybridization (FISH). The methods of the present invention may also include staining the tissue sample with one or more antibodies specific for melanoma. The antibody may be S100, gp100 (HMB-45 antibody), MART-1/Melan-A, MITF, or tyrosinase antibodies, or a cocktail of all three antibodies. Alternatively, the methods may further comprise fluorescence in situ hybridization (FISH), comparative genomic hybridization (CGH), or gene expression analysis.
  • Moreover, the invention also includes measuring transcription of genes or the translation of proteins that are indirectly or directly under the influence of a gene hyper- or hypomethylated in melanoma. Specifically, the invention includes using antibodies or probes or primers to measure FRZB, GSTM2, KCNK4, NPR2, or TRIP6 proteins or nucleic acids, wherein reduced levels are indicative of melanoma. The levels relative to a benign control may be about 80%, preferably 50%, more preferably 25-0%. Alternatively, antibodies or probes or primers to measure CARD15, CCL3, CD2, EMR3, EVI2A, HLA-DPA1, IFNG, ITK, KLK10, LAT, MPO, OSM, PSCA, PTHLH, PTHR1, RUNX3, or TNFSF8 proteins or nucleic acids, wherein elevated levels are is indicative of melanoma. The levels relative to a benign control may be 110%, more preferably 150%, more preferably 200-500% (i.e., two to five fold higher relative to the control), more preferably 1000-3000% higher.
  • In other non-limiting embodiments, the present invention provides a kit comprising: (a) at least one reagent selected from the group consisting of: (i) a nucleic acid probe capable of specifically hybridizing with a regulatory element differentially methylated in melanoma and benign nevi; (ii) a pair of nucleic acid primers capable of PCR amplification of a regulatory element differentially methylated in melanoma and benign nevi; and (iii) a methylation specific antibody and a probe capable of specifically hybridizing with a regulatory element differentially methylated in melanoma and benign nevi; and (b) instructions for use in measuring a level of methylation of at least one regulatory element in a tissue sample from a subject suspected of having melanoma.
  • In other non-limiting embodiments, the present invention provides a method of identifying a compound that prevents or treats melanoma progression, the method comprising the steps of: (a) contacting a compound with a sample comprising a cell or a tissue; (b) measuring a level of methylation of one or more regulatory elements differentially methylated in melanoma and benign nevi; and (c) determining a functional effect of the compound on the level of methylation; thereby identifying a compound that prevents or treats melanoma.
    • 4. BRIEF DESCRIPTION OF THE FIGURES
  • FIGS. 1A-1I show correlation curves showing the reproducibility and effects of formalin fixation and normal cell contamination on melanocytic methylation profiles obtained with the Illumina GoldenGate methylation array. FIGS. 1A-1C show the reproducibility and effects of formalin fixation on methylation profile. Shown are non-fixed duplicates of the MCF-7 breast cancer cell line (r2=0.98) (FIG. 1A), duplicates of the Mel-505 melanoma cell line (r2=0.99) (FIG. 1B), and comparison of formalin-fixed, paraffin-embedded Mel-505 with non-fixed Mel-505 cells (r2=0.99) (FIG. 1C). FIGS. 1D-II show the effect of contamination with increasing proportions of normal peripheral blood leukocyte (PBL) DNA on the Mel-505 melanoma cell methylation profile. Shown are Mel-505 cells that were mixed with PBL DNA in the following proportions: 100% Mel-505, (FIG. 1D); 90% Mel-505/10% PBL (FIG. 1E); 80% Mel-505/20% PBL (FIG. 1F); 70% Mel-505/30% PBL (FIG. 1G); 60% Mel-505/40% PBL (FIG. 1H); and 50% Mel-505/50% PBL (FIG. 1I).
  • FIGS. 2A and 2B show the hierarchical clustering of methylation β values using the Illumina GoldenGate Cancer Panel I array in FFPE benign nevi and malignant melanomas. DNA methylation profiles for 22 melanomas and 27 nevi are shown. Columns represent tissue samples; rows represent CpG loci. The methylation levels (β) range from 0 (very light grey/unmethylated) to 1 (dark grey/highly methylated). Missing values are shown in white. FIGS. 2A and 2B display clusters based on the 29 CpG sites/genes showing significantly different methylation β levels between moles and melanomas after adjustment for age and sex and Bonferroni correction for multiple comparisons. The upper portion of the heatmap shows 7 CpG loci in 6 genes exhibiting hypermethylation and 22 CpG loci in 18 genes exhibiting hypomethylation in melanomas compared with moles.
  • FIGS. 3A-3L show box plots of methylation β levels in the 12 CpG loci identified by PAM analysis that predict melanoma. The loci shown differed by >0.2 mean β between melanomas and moles, except for ITK_P114_F. Each box plot shows the mean β value (dark bar within box), the standard deviation (outer boundaries of box), and the range of β values (broken line) within the melanomas or nevus groups. Additional information on mean β values for nevi and melanomas, differences in mean β values, and p-values adjusted for age, sex, and multiple comparisons through Bonferroni correction are given in Table 3A.
  • FIG. 4A-4O show ROC curves showing the sensitivity and specificity of selected CpG loci to distinguish melanomas from benign nevi based on methylation level. The area under the curve (AUC) is presented, showing sensitivity and specificity of melanoma diagnosis for CpG sites that exhibited either significant hypomethylation (n=22) or hypermethylation (n=7) in melanomas compared with benign nevi after adjustment for age, sex and multiple comparisons. Sensitivity, or the frequency of detection of true positives (melanoma vs nevus), is shown along the y axis, while specificity, or the frequency of false positives, is shown along the x axis. The calculated AUC is given for each plot.
  • FIG. 5 shows a Venn diagram of CpG sites that significantly differentiate non-dysplastic and dysplastic nevi from primary melanomas or metastases.
    •  5. DETAILED DESCRIPTION OF THE INVENTION 5.1. Definitions
  • The term “melanoma” refers to malignant neoplasms of melanocytes, which are pigment cells present normally in the epidermis, in adnexal structures including hair follicles, and sometimes in the dermis, as well as extracutaneous sites such as the mucosa, meninx, conjuctiva, and uvea. Sometimes it is referred to as “cutaneous melanoma” or “malignant melanoma.” There are at least four types of cutaneous melanoma: lentigo maligna melanoma (LMM), superficial spreading melanoma (SSM), nodular melanoma (NM), and acral lentiginous melanoma (ALM). Cutaneous melanoma typically starts as a proliferation of single melanocytes, e.g., at the junction of the epidermis and the dermis. The cells first grow in a horizontal manner and settle in an area of the skin that can vary from a few millimeters to several centimeters. As noted above, in most instances the transformed melanocytes produce increased amounts of pigment so that the area involved can be seen by the clinician.
  • The terms “nucleic acid” and “nucleic acid molecule” may be used interchangeably throughout the disclosure. The terms refer to nucleic acids of any composition from, such as DNA (e.g., complementary DNA (cDNA), genomic DNA (gDNA) and the like), RNA (e.g., messenger RNA (mRNA), short inhibitory RNA (siRNA), ribosomal RNA (rRNA), tRNA, microRNA, RNA highly expressed by the melanoma or nevi, and the like), and/or DNA or RNA analogs (e.g., containing base analogs, sugar analogs and/or a non-native backbone and the like), RNA/DNA hybrids and polyamide nucleic acids (PNAs), all of which can be in single- or double-stranded form, and unless otherwise limited, can encompass known analogs of natural nucleotides that can function in a similar manner as naturally occurring nucleotides. Examples of nucleic acids are SEQ ID Nos. 1-75 shown in Table 4A and Table 4B; SEQ ID Nos. 76-93 in Table 7A and 7B; SEQ ID Nos. 94-265 in Table 9D; SEQ ID Nos. 266-283 in Table 13; SEQ ID Nos. 284-339 in Table 14; and SEQ ID Nos. 340-353 in Table 15, which may be methylated or unmethylated at any CpG site present in the sequence, including the CpG sites shown in brackets on some sequences. A template nucleic acid in some embodiments can be from a single chromosome (e.g., a nucleic acid sample may be from one chromosome of a sample obtained from a diploid organism). Unless specifically limited, the term encompasses nucleic acids containing known analogs of natural nucleotides that have similar binding properties as the reference nucleic acid and are metabolized in a manner similar to naturally occurring nucleotides. Unless otherwise indicated, a particular nucleic acid sequence also implicitly encompasses methylated forms, conservatively modified variants thereof (e.g., degenerate codon substitutions), alleles, orthologs, single nucleotide polymorphisms (SNPs), and complementary sequences as well as the sequence explicitly indicated. The term nucleic acid is used interchangeably with locus, gene, cDNA, and mRNA encoded by a gene. The term also may include, as equivalents, derivatives, variants and analogs of RNA or DNA synthesized from nucleotide analogs, single-stranded (“sense” or “antisense”, “plus” strand or “minus” strand, “forward” reading frame or “reverse” reading frame) and double-stranded polynucleotides. Deoxyribonucleotides include deoxyadenosine, deoxycytidine, deoxyguanosine and deoxythymidine. For RNA, the base cytosine is replaced with uracil.
  • A “methylated regulatory element” as used herein refers to a segment of DNA sequence at a defined location in the genome of an individual. Typically, a “methylated regulatory element” is at least 15 nucleotides in length and contains at least one cytosine. It may be at least 18, 20, 25, 30, 50, 80, 100, 150, 200, 250, or 300 nucleotides in length and contain 1 or 2, 5, 10, 15, 20, 25, or 30 cytosines. For any one “methylated regulatory element” at a given location, e.g., within a region centering around a given genetic locus, nucleotide sequence variations may exist from individual to individual and from allele to allele even for the same individual. Typically, such a region centering around a defined genetic locus (e.g., a CpG island) contains the locus as well as upstream and/or downstream sequences. Each of the upstream or downstream sequence (counting from the 5′ or 3′ boundary of the genetic locus, respectively) can be as long as 10 kb, in other cases may be as long as 5 kb, 2 kb, 1 kb, 500 bp, 200 bp, or 100 bp. Furthermore, a “methylated regulatory element” may modulate expression of a nucleotide sequence transcribed into a protein or not transcribed for protein production (such as a non-coding mRNA). The “methylated regulatory element” may be an inter-gene sequence, intra-gene sequence (intron), protein-coding sequence (exon), a non protein-coding sequence (such as a transcription promoter or enhancer), or a combination thereof.
  • As used herein, a “methylated nucleotide” or a “methylated nucleotide base” refers to the presence of a methyl moiety on a nucleotide base, where the methyl moiety is not present in a recognized typical nucleotide base. For example, cytosine does not contain a methyl moiety on its pyrimidine ring, but 5-methylcytosine contains a methyl moiety at position 5 of its pyrimidine ring. Therefore, cytosine is not a methylated nucleotide and 5-methylcytosine is a methylated nucleotide. In another example, thymine contains a methyl moiety at position 5 of its pyrimidine ring, however, for purposes herein, thymine is not considered a methylated nucleotide when present in DNA since thymine is a typical nucleotide base of DNA. Typical nucleoside bases for DNA are thymine, adenine, cytosine and guanine. Typical bases for RNA are uracil, adenine, cytosine and guanine. Correspondingly a “methylation site” is the location in the target gene nucleic acid region where methylation has, or has the possibility of occurring. For example a location containing CpG is a methylation site wherein the cytosine may or may not be methylated.
  • As used herein, a “CpG site” or “methylation site” is a nucleotide within a nucleic acid that is susceptible to methylation either by natural occurring events in vivo or by an event instituted to chemically methylate the nucleotide in vitro.
  • As used herein, a “methylated nucleic acid molecule” refers to a nucleic acid molecule that contains one or more nucleotides that is/are methylated.
  • A “CpG island” as used herein describes a segment of DNA sequence that comprises a functionally or structurally deviated CpG density. For example, Yamada et al. have described a set of standards for determining a CpG island: it must be at least 400 nucleotides in length, has a greater than 50% GC content, and an OCF/ECF ratio greater than 0.6 (Yamada et al., 2004, Genome Research, 14, 247-266). Others have defined a CpG island less stringently as a sequence at least 200 nucleotides in length, having a greater than 50% GC content, and an OCF/ECF ratio greater than 0.6 (Takai et al., 2002, Proc. Natl. Acad. Sci. USA, 99, 3740-3745).
  • The term “epigenetic state” or “epigenetic status” as used herein refers to any structural feature at a molecular level of a nucleic acid (e.g., DNA or RNA) other than the primary nucleotide sequence. For instance, the epigenetic state of a genomic DNA may include its secondary or tertiary structure determined or influenced by, e.g., its methylation pattern or its association with cellular proteins.
  • The term “methylation profile” “methylation state” or “methylation status,” as used herein to describe the state of methylation of a genomic sequence, refers to the characteristics of a DNA segment at a particular genomic locus relevant to methylation. Such characteristics include, but are not limited to, whether any of the cytosine (C) residues within this DNA sequence are methylated, location of methylated C residue(s), percentage of methylated C at any particular stretch of residues, and allelic differences in methylation due to, e.g., difference in the origin of the alleles. The term “methylation” profile” or “methylation status” also refers to the relative or absolute concentration of methylated C or unmethylated C at any particular stretch of residues in a biological sample. For example, if cytosine (C) residue(s) not typically methylated within a DNA sequence are methylated, it may be referred to as “hypermethylated”; whereas if cytosine (C) residue(s) typically methylated within a DNA sequence are not methylated, it may be referred to as “hypomethylated”. Likewise, if the cytosine (C) residue(s) within a DNA sequence (e.g., sample nucleic acid) are methylated as compared to another sequence from a different region or from a different individual (e.g., relative to normal nucleic acid), that sequence is considered hypermethylated compared to the other sequence. Alternatively, if the cytosine (C) residue(s) within a DNA sequence are not methylated as compared to another sequence from a different region or from a different individual, that sequence is considered hypomethylated compared to the other sequence. These sequences are said to be “differentially methylated”, and more specifically, when the methylation status differs between melanoma and benign or healthy moles, the sequences are considered “differentially methylated in melanoma and benign nevi”. Measurement of the levels of differential methylation may be done by a variety of ways known to those skilled in the art. One method is to measure the ratio of methylated to unmethylated alleles or β-value (see section 6.5 below). The difference in the ratios between methylated and unmethylated sequences in melanoma and benign nevi may be 0.1, 0.15, 0.2, 0.25, 0.3, 0.4, 0.5, 0.55, 0.6, 0.65, 0.7, 0.8, or 0.9. In non-limiting embodiments, the difference in the ratios is between 0.2 and 0.65, or between 0.2 and 0.4.
  • The term “agent that binds to methylated nucleotides” as used herein refers to a substance that is capable of binding to methylated nucleic acid. The agent may be naturally-occurring or synthetic, and may be modified or unmodified. In one embodiment, the agent allows for the separation of different nucleic acid species according to their respective methylation states. An example of an agent that binds to methylated nucleotides is described in PCT Pub. No. WO 2006/056480 A2 (Rehli), hereby incorporated by reference in its entirety. The described agent is a bifunctional polypeptide comprising the DNA-binding domain of a protein belonging to the family of Methyl-CpG binding proteins (MBDs) and an Fc portion of an antibody. The recombinant methyl-CpG-binding, antibody-like protein can preferably bind CpG methylated DNA in an antibody-like manner. That means, the methyl-CpG-binding, antibody-like protein has a high affinity and high avidity to its “antigen”, which is preferably DNA that is methylated at CpG dinucleotides. The agent may also be a multivalent MBD.
  • The term “bisulfite” as used herein encompasses any suitable type of bisulfite, such as sodium bisulfite, or other chemical agent that is capable of chemically converting a cytosine (C) to a uracil (U) without chemically modifying a methylated cytosine and therefore can be used to differentially modify a DNA sequence based on the methylation status of the DNA, e.g., U.S. Pat. Pub. US 2010/0112595 (Menchen et al.). As used herein, a reagent that “differentially modifies” methylated or non-methylated DNA encompasses any reagent that modifies methylated and/or unmethylated DNA in a process through which distinguishable products result from methylated and non-methylated DNA, thereby allowing the identification of the DNA methylation status. Such processes may include, but are not limited to, chemical reactions (such as a C→U conversion by bisulfite) and enzymatic treatment (such as cleavage by a methylation-dependent endonuclease). Thus, an enzyme that preferentially cleaves or digests methylated DNA is one capable of cleaving or digesting a DNA molecule at a much higher efficiency when the DNA is methylated, whereas an enzyme that preferentially cleaves or digests unmethylated DNA exhibits a significantly higher efficiency when the DNA is not methylated.
  • The terms “non-bisulfite-based method” and “non-bisulfite-based quantitative method” as used herein refer to any method for quantifying methylated or non-methylated nucleic acid that does not require the use of bisulfite. The terms also refer to methods for preparing a nucleic acid to be quantified that do not require bisulfite treatment. Examples of non-bisulfite-based methods include, but are not limited to, methods for digesting nucleic acid using one or more methylation sensitive enzymes and methods for separating nucleic acid using agents that bind nucleic acid based on methylation status. The terms “methyl-sensitive enzymes” and “methylation sensitive restriction enzymes” are DNA restriction endonucleases that are dependent on the methylation state of their DNA recognition site for activity. For example, there are methyl-sensitive enzymes that cleave or digest at their DNA recognition sequence only if it is not methylated. Thus, an unmethylated DNA sample will be cut into smaller fragments than a methylated DNA sample. Similarly, a hypermethylated DNA sample will not be cleaved. In contrast, there are methyl-sensitive enzymes that cleave at their DNA recognition sequence only if it is methylated. As used herein, the terms “cleave”, “cut” and “digest” are used interchangeably.
  • The term “target nucleic acid” as used herein refers to a nucleic acid examined using the methods disclosed herein to determine if the nucleic acid is melanoma associated. The term “control nucleic acid” as used herein refers to a nucleic acid used as a reference nucleic acid according to the methods disclosed herein to determine if the nucleic acid is associated with melanoma. The term “gene” means the segment of DNA involved in producing a polypeptide chain; it includes regions preceding and following the coding region (leader and trailer) involved in the transcription/translation of the gene product and the regulation of the transcription/translation, as well as intervening sequences (introns) between individual coding segments (exons).
  • In this application, the terms “polypeptide,” “peptide,” and “protein” are used interchangeably herein to refer to a polymer of amino acid residues. The terms apply to amino acid polymers in which one or more amino acid residue is an artificial chemical mimetic of a corresponding naturally occurring amino acid, as well as to naturally occurring amino acid polymers and non-naturally occurring amino acid polymers. As used herein, the terms encompass amino acid chains of any length, including full-length proteins (i.e., antigens), wherein the amino acid residues are linked by covalent peptide bonds.
  • The term “amino acid” refers to naturally occurring and synthetic amino acids, as well as amino acid analogs and amino acid mimetics that function in a manner similar to the naturally occurring amino acids. Naturally occurring amino acids are those encoded by the genetic code, as well as those amino acids that are later modified, e.g., hydroxyproline, gamma-carboxyglutamate, and 0-phosphoserine Amino acids may be referred to herein by either the commonly known three letter symbols or by the one-letter symbols recommended by the IUPAC-IUB Biochemical Nomenclature Commission. Nucleotides, likewise, may be referred to by their commonly accepted single-letter codes.
  • “Primers” as used herein refer to oligonucleotides that can be used in an amplification method, such as a polymerase chain reaction (PCR), to amplify a nucleotide sequence based on the polynucleotide sequence corresponding to a particular genomic sequence, e.g., one specific for a particular CpG site. At least one of the PCR primers for amplification of a polynucleotide sequence is sequence-specific for the sequence.
  • The term “template” refers to any nucleic acid molecule that can be used for amplification in the technology. RNA or DNA that is not naturally double stranded can be made into double stranded DNA so as to be used as template DNA. Any double stranded DNA or preparation containing multiple, different double stranded DNA molecules can be used as template DNA to amplify a locus or loci of interest contained in the template DNA.
  • The term “amplification reaction” as used herein refers to a process for copying nucleic acid one or more times. In embodiments, the method of amplification includes, but is not limited to, polymerase chain reaction, self-sustained sequence reaction, ligase chain reaction, rapid amplification of cDNA ends, polymerase chain reaction and ligase chain reaction, Q-P replicase amplification, strand displacement amplification, rolling circle amplification, or splice overlap extension polymerase chain reaction. In some embodiments, a single molecule of nucleic acid may be amplified.
  • The term “sensitivity” as used herein refers to the number of true positives divided by the number of true positives plus the number of false negatives, where sensitivity (sens) may be within the range of 0<sens<1. Ideally, method embodiments herein have the number of false negatives equaling zero or close to equaling zero, so that no subject is wrongly identified as not having melanoma when they indeed have melanoma. Conversely, an assessment often is made of the ability of a prediction algorithm to classify negatives correctly, a complementary measurement to sensitivity. The term “specificity” as used herein refers to the number of true negatives divided by the number of true negatives plus the number of false positives, where sensitivity (spec) may be within the range of 0<spec<1. Ideally, the methods described herein have the number of false positives equaling zero or close to equaling zero, so that no subject is wrongly identified as having melanoma when they do not in fact have melanoma. Hence, a method that has both sensitivity and specificity equaling one, or 100%, is preferred.
  • “RNAi molecule” or “siRNA” refers to a nucleic acid that forms a double stranded RNA, which double stranded RNA has the ability to reduce or inhibit expression of a gene or target gene when the siRNA expressed in the same cell as the gene or target gene. “siRNA” thus refers to the double stranded RNA formed by the complementary strands. The complementary portions of the siRNA that hybridize to form the double stranded molecule typically have substantial or complete identity. In one embodiment, siRNA refers to a nucleic acid that has substantial or complete identity to a target gene and forms a double stranded siRNA. The sequence of the siRNA can correspond to the full length target gene, or a subsequence thereof. Typically, the siRNA is at least about 15-50 nucleotides in length (e.g., each complementary sequence of the double stranded siRNA is 15-50 nucleotides in length, and the double stranded siRNA is about 15-50 base pairs in length, preferable about preferably about 20-30 base nucleotides, preferably about 20-25 nucleotides in length, e.g., 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30 nucleotides in length.
  • An “antisense” polynucleotide is a polynucleotide that is substantially complementary to a target polynucleotide and has the ability to specifically hybridize to the target polynucleotide. Ribozymes are enzymatic RNA molecules capable of catalyzing specific cleavage of RNA. The composition of ribozyme molecules preferably includes one or more sequences complementary to a target mRNA, and the well-known catalytic sequence responsible for mRNA cleavage or a functionally equivalent sequence (see, e.g., U.S. Pat. No. 5,093,246 (Cech et al.); U.S. Pat. No. 5,766,942 (Haseloff et al.); U.S. Pat. No. 5,856,188 (Hampel et al.) which are incorporated herein by reference in their entirety). Ribozyme molecules designed to catalytically cleave target mRNA transcripts can also be used to prevent translation of genes associated with the progression of melanoma. These genes may be genes found to be hypomethylated in melanoma.
  • The phrase “functional effects” in the context of assays for testing means compounds that modulate a methylation of a regulatory region of a gene associated with melanoma. This may also be a chemical or phenotypic effect such as altered transcriptional activity of a gene hyper- or hypomethylated in melanoma, or altered activities and the downstream effects of proteins encoded by these genes. A functional effect may include transcriptional activation or repression, the ability of cells to proliferate, expression in cells during melanoma progression, and other characteristics of melanoma cells. “Functional effects” include in vitro, in vivo, and ex vivo activities. By “determining the functional effect” is meant assaying for a compound that increases or decreases the transcription of genes or the translation of proteins that are indirectly or directly under the influence of a gene hyper- or hypomethylated in melanoma. Such functional effects can be measured by any means known to those skilled in the art, e.g., changes in spectroscopic characteristics (e.g., fluorescence, absorbance, refractive index); hydrodynamic (e.g., shape), chromatographic; or solubility properties for the protein; ligand binding assays, e.g., binding to antibodies; measuring inducible markers or transcriptional activation of the marker; measuring changes in enzymatic activity; the ability to increase or decrease cellular proliferation, apoptosis, cell cycle arrest, measuring changes in cell surface markers. Validation the functional effect of a compound on melanoma progression can also be performed using assays known to those of skill in the art such as metastasis of melanoma cells by tail vein injection of melanoma cells in mice. The functional effects can be evaluated by many means known to those skilled in the art, e.g., microscopy for quantitative or qualitative measures of alterations in morphological features, measurement of changes in RNA or protein levels for other genes expressed in melanoma cells, measurement of RNA stability, identification of downstream or reporter gene expression (CAT, luciferase, β-gal, GFP and the like), e.g., via chemiluminescence, fluorescence, colorimetric reactions, antibody binding, inducible markers, etc.
  • “Inhibitors,” “activators,” and “modulators” of the markers are used to refer to activating, inhibitory, or modulating molecules identified using in vitro and in vivo assays of the methylation state, the expression of genes hyper- or hypomethylated in melanoma or the translation proteins encoded thereby Inhibitors, activators, or modulators also include naturally occurring and synthetic ligands, antagonists, agonists, antibodies, peptides, cyclic peptides, nucleic acids, antisense molecules, ribozymes, RNAi molecules, small organic molecules and the like. Such assays for inhibitors and activators include, e.g., (1)(a) measuring methylation states, (b) the mRNA expression, or (c) proteins expressed by genes hyper- or hypomethylated in melanoma in vitro, in cells, or cell extracts; (2) applying putative modulator compounds; and (3) determining the functional effects on activity, as described above.
  • Samples or assays comprising genes hyper- or hypomethylated in melanoma are treated with a potential activator, inhibitor, or modulator are compared to control samples without the inhibitor, activator, or modulator to examine the extent of inhibition. Control samples (untreated with inhibitors) are assigned a relative activity value of 100% Inhibition of methylation, expression, or proteins encoded by genes hyper- or hypomethylated in melanoma is achieved when the activity value relative to the control is about 80%, preferably 50%, more preferably 25-0%. Activation of methylation, expression, or proteins encoded by genes hyper- or hypomethylated in melanoma is achieved when the activity value relative to the control (untreated with activators) is 110%, more preferably 150%, more preferably 200-500% (i.e., two to five fold higher relative to the control), more preferably 1000-3000% higher.
  • The term “test compound” or “drug candidate” or “modulator” or grammatical equivalents as used herein describes any molecule, either naturally occurring or synthetic, e.g., protein, oligopeptide, small organic molecule, polysaccharide, peptide, circular peptide, lipid, fatty acid, siRNA, polynucleotide, oligonucleotide, etc., to be tested for the capacity to directly or indirectly modulate genes hyper- or hypomethylated in melanoma. The test compound can be in the form of a library of test compounds, such as a combinatorial or randomized library that provides a sufficient range of diversity. Test compounds are optionally linked to a fusion partner, e.g., targeting compounds, rescue compounds, dimerization compounds, stabilizing compounds, addressable compounds, and other functional moieties. Conventionally, new chemical entities with useful properties are generated by identifying a test compound (called a “lead compound”) with some desirable property or activity, e.g., inhibiting activity, creating variants of the lead compound, and evaluating the property and activity of those variant compounds. Often, high throughput screening (HTS) methods are employed for such an analysis. The compound may be “small organic molecule” that is an organic molecule, either naturally occurring or synthetic, that has a molecular weight of more than about 50 daltons and less than about 2500 daltons, preferably less than about 2000 daltons, preferably between about 100 to about 1000 daltons, more preferably between about 200 to about 500 daltons.
    • 5.2. Tissue Samples
  • The tissue sample may be from a patient suspected of having melanoma or from a patient diagnosed with melanoma, e.g., for confirmation of diagnosis or establishing a clear margin or for the detection of melanoma cells in other tissues such as lymph nodes. The biological sample may also be from a subject with an ambiguous diagnosis in order to clarify the diagnosis. The sample may be obtained for the purpose of differential diagnosis, e.g., a subject with a histopathologically benign lesion to confirm the diagnosis. The sample may also be obtained for the purpose of prognosis, i.e., determining the course of the disease and selecting primary treatment options. Tumor staging and grading are examples of prognosis. The sample may also be evaluated to select or monitor therapy, selecting likely responders in advance from non-responders or monitoring response in the course of therapy. In addition, the sample may be evaluated as part of post-treatment ongoing surveillance of patients who have had melanoma. The sample may also be obtained to differentiate dysplastic nevi from other benign nevi. The sample may be a melanoma sample such as a melanomas will be superficial spreading melanoma, nodular melanoma, lentigo maligna melanoma, acral lentiginous melanoma, unclassifiable or other (spitzoid/desmoplastic/nevoid/spindle cell) melanoma. The sample may be normal skin, a benign nevi, a melanoma-in-situs (MIS), or a high-grade dysplastic nevi (HGDN).
  • Biological samples may be obtained using any of a number of methods in the art. Examples of biological samples comprising potential melanocytic lesions include those obtained from excised skin biopsies, such as punch biopsies, shave biopsies, fine needle aspirates (FNA), or surgical excisions; or biopsy from non-cutaneous tissues such as lymph node tissue, mucosa, conjuctiva, or uvea, other embodiments. The biological sample can be obtained by shaving, waxing, or stripping the region of interest on the skin. A non-limiting example of a product for stripping skin for RNA recovery is the EGIR′ tape strip product (DermTech International, La Jolla, Calif., see also, Wachsman et al., 2011, Brit. J. Derm. 164 797-806). Representative biopsy techniques include, but are not limited to, excisional biopsy, incisional biopsy, needle biopsy, surgical biopsy. An “excisional biopsy” refers to the removal of an entire tumor mass with a small margin of normal tissue surrounding it. An “incisional biopsy” refers to the removal of a wedge of tissue that includes a cross-sectional diameter of the tumor. A diagnosis or prognosis made by endoscopy or fluoroscopy can require a “core-needle biopsy” of the tumor mass, or a “fine-needle aspiration biopsy” which generally contains a suspension of cells from within the tumor mass. The biological sample may be a microdissected sample, such as a PALM-laser (Carl Zeiss MicroImaging GmbH, Germany) capture microdissected sample.
  • A sample may also be a sample of muscosal surfaces, blood and blood fractions or products (e.g., serum, plasma, platelets, red blood cells, white blood cells, circulating tumor cells isolated from blood, free DNA isolated from blood, and the like), sputum, lymph and tongue tissue, cultured cells, e.g., primary cultures, explants, and transformed cells, stool, urine, etc. The sample may also be vascular tissue or cells from blood vessels such as microdissected blood vessel cells of endothelial origin. A sample is typically obtained from a eukaryotic organism, most preferably a mammal such as a primate e.g., chimpanzee or human; cow; dog; cat; a rodent, e.g., guinea pig; rat; mouse; rabbit.
  • A sample can be treated with a fixative such as formaldehyde and embedded in paraffin (FFPE) and sectioned for use in the methods of the invention. Alternatively, fresh or frozen tissue may be used. These cells may be fixed, e.g., in alcoholic solutions such as 100% ethanol or 3:1 methanol:acetic acid. Nuclei can also be extracted from thick sections of paraffin-embedded specimens to reduce truncation artifacts and eliminate extraneous embedded material. Typically, biological samples, once obtained, are harvested and processed prior to hybridization using standard methods known in the art. Such processing typically includes protease treatment and additional fixation in an aldehyde solution such as formaldehyde.
    • 5.3. Techniques for Measuring Methylation
  • A variety of methylation analysis procedures are known in the art and may be used to practice the invention. These assays allow for determination of the methylation state of one or a plurality of CpG sites within a tissue sample. In addition, these methods may be used for absolute or relative quantification of methylated nucleic acids. Another embodiment of the invention are methods of detecting melanoma based on the differentially methylated sites found in tissue analysis described herein, and not differentially methylated in cultured melanocytes and/or melanoma cell lines. Such methylation assays involve, among other techniques, two major steps. The first step is a methylation specific reaction or separation, such as (i) bisulfite treatment, (ii) methylation specific binding, or (iii) methylation specific restriction enzymes. The second major step involves (i) amplification and detection, or (ii) direct detection, by a variety of methods such as (a) PCR (sequence-specific amplification) such as Taqman(91, (b) DNA sequencing of untreated and bisulfite-treated DNA, (c) sequencing by ligation of dye-modified probes (including cyclic ligation and cleavage), (d) pyrosequencing, (e) single-molecule sequencing, (f) mass spectroscopy, or (g) Southern blot analysis.
  • Additionally, restriction enzyme digestion of PCR products amplified from bisulfite-converted DNA may be used, e.g., the method described by Sadri & Hornsby (1996, Nucl. Acids Res. 24:5058-5059), or COBRA (Combined Bisulfite Restriction Analysis) (Xiong & Laird, 1997, Nucleic Acids Res. 25:2532-2534). COBRA analysis is a quantitative methylation assay useful for determining DNA methylation levels at specific gene loci in small amounts of genomic DNA. Briefly, restriction enzyme digestion is used to reveal methylation-dependent sequence differences in PCR products of sodium bisulfite-treated DNA. Methylation-dependent sequence differences are first introduced into the genomic DNA by standard bisulfite treatment according to the procedure described by Frommer et al. (Frommer et al., 1992, Proc. Nat. Acad. Sci. USA, 89, 1827-1831). PCR amplification of the bisulfite converted DNA is then performed using primers specific for the CpG sites of interest, followed by restriction endonuclease digestion, gel electrophoresis, and detection using specific, labeled hybridization probes. Methylation levels in the original DNA sample are represented by the relative amounts of digested and undigested PCR product in a linearly quantitative fashion across a wide spectrum of DNA methylation levels. In addition, this technique can be reliably applied to DNA obtained from microdissected paraffin-embedded tissue samples. Typical reagents (e.g., as might be found in a typical COBRA-based kit) for COBRA analysis may include, but are not limited to: PCR primers for specific gene (or methylation-altered DNA sequence or CpG island); restriction enzyme and appropriate buffer; gene-hybridization oligo; control hybridization oligo; kinase labeling kit for oligo probe; and radioactive nucleotides. Additionally, bisulfite conversion reagents may include: DNA denaturation buffer; sulfonation buffer; DNA recovery reagents or kits (e.g., precipitation, ultrafiltration, affinity column); desulfonation buffer; and DNA recovery components.
    • 5.3.1. Methylation-Specific PCR (MSP)
  • Methylation-Specific PCR (MSP) allows for assessing the methylation status of virtually any group of CpG sites within a CpG island, independent of the use of methylation-sensitive restriction enzymes (Herman et al., 1996, Proc. Nat. Acad. Sci. USA, 93, 9821-9826; U.S. Pat. Nos. 5,786,146, 6,017,704, 6,200,756, 6,265,171 (Herman & Baylin) U.S. Pat. Pub. No. 2010/0144836 (Van Engeland et al.); which are hereby incorporated by reference in their entirety). Briefly, DNA is modified by sodium bisulfite converting unmethylated, but not methylated cytosines to uracil, and subsequently amplified with primers specific for methylated versus unmethylated DNA. MSP requires only small quantities of DNA, is sensitive to 0.1% methylated alleles of a given CpG island locus, and can be performed on DNA extracted from paraffin-embedded samples. Typical reagents (e.g., as might be found in a typical MSP-based kit) for MSP analysis may include, but are not limited to: methylated and unmethylated PCR primers for specific gene (or methylation-altered DNA sequence or CpG island), optimized PCR buffers and deoxynucleotides, and specific probes. The ColoSure™ test is a commercially available test for colon cancer based on the MSP technology and measurement of methylation of the vimentin gene (Itzkowitz et al., 2007, Clin Gastroenterol. Hepatol. 5(1), 111-117). Alternatively, one may use quantitative multiplexed methylation specific PCR (QM-PCR), as described by Fackler et al. Fackler et al., 2004, Cancer Res. 64(13) 4442-4452; or Fackler et al., 2006, Clin. Cancer Res. 12(11 Pt 1) 3306-3310.
    • 5.3.2. MethyLight and Heavy Methyl Methods
  • The MethyLight and Heavy Methyl assays are a high-throughput quantitative methylation assay that utilizes fluorescence-based real-time PCR (Taq Man®) technology that requires no further manipulations after the PCR step (Eads, C. A. et al., 2000, Nucleic Acid Res. 28, e 32; Cottrell et al., 2007, J. Urology 177, 1753, U.S. Pat. No. 6,331,393 (Laird et al.), the contents of which are hereby incorporated by reference in their entirety). Briefly, the MethyLight process begins with a mixed sample of genomic DNA that is converted, in a sodium bisulfite reaction, to a mixed pool of methylation-dependent sequence differences according to standard procedures (the bisulfite process converts unmethylated cytosine residues to uracil). Fluorescence-based PCR is then performed either in an “unbiased” (with primers that do not overlap known CpG methylation sites) PCR reaction, or in a “biased” (with PCR primers that overlap known CpG dinucleotides) reaction. Sequence discrimination can occur either at the level of the amplification process or at the level of the fluorescence detection process, or both. The MethyLight assay may be used as a quantitative test for methylation patterns in the genomic DNA sample, wherein sequence discrimination occurs at the level of probe hybridization. In this quantitative version, the PCR reaction provides for unbiased amplification in the presence of a fluorescent probe that overlaps a particular putative methylation site. An unbiased control for the amount of input DNA is provided by a reaction in which neither the primers, nor the probe overlie any CpG dinucleotides. Alternatively, a qualitative test for genomic methylation is achieved by probing of the biased PCR pool with either control oligonucleotides that do not “cover” known methylation sites (a fluorescence-based version of the “MSP” technique), or with oligonucleotides covering potential methylation sites. Typical reagents (e.g., as might be found in a typical MethyLight-based kit) for MethyLight analysis may include, but are not limited to: PCR primers for specific gene (or methylation-altered DNA sequence or CpG island); TaqMan® probes; optimized PCR buffers and deoxynucleotides; and Taq polymerase. The MethyLight technology is used for the commercially available tests for lung cancer (epi proLung BL Reflex Assay); colon cancer (epi proColon assay and mSEPT9 assay) (Epigenomics, Berlin, Germany) PCT Pub. No. WO 2003/064701 (Schweikhardt and Sledziewski), the contents of which is hereby incorporated by reference in its entirety.
  • Quantitative MethyLight uses bisulfite to convert genomic DNA and the methylated sites are amplified using PCR with methylation independent primers. Detection probes specific for the methylated and unmethylated sites with two different fluorophores provides simultaneous quantitative measurement of the methylation. The Heavy Methyl technique begins with bisulfate conversion of DNA. Next specific blockers prevent the amplification of unmethylated DNA. Methylated genomic DNA does not bind the blockers and their sequences will be amplified. The amplified sequences are detected with a methylation specific probe. (Cottrell et al., 2004, Nuc. Acids Res. 32, e10, the contents of which is hereby incorporated by reference in its entirety).
  • The Ms-SNuPE technique is a quantitative method for assessing methylation differences at specific CpG sites based on bisulfite treatment of DNA, followed by single-nucleotide primer extension (Gonzalgo & Jones, 1997, Nucleic Acids Res. 25, 2529-2531). Briefly, genomic DNA is reacted with sodium bisulfite to convert unmethylated cytosine to uracil while leaving 5-methylcytosine unchanged. Amplification of the desired target sequence is then performed using PCR primers specific for bisulfite-converted DNA, and the resulting product is isolated and used as a template for methylation analysis at the CpG site(s) of interest. Small amounts of DNA can be analyzed (e.g., microdissected pathology sections), and it avoids utilization of restriction enzymes for determining the methylation status at CpG sites. Typical reagents (e.g., as might be found in a typical Ms-SNuPE-based kit) for Ms-SNuPE analysis may include, but are not limited to: PCR primers for specific gene (or methylation-altered DNA sequence or CpG island); optimized PCR buffers and deoxynucleotides; gel extraction kit; positive control primers; Ms-SNuPE primers for specific gene; reaction buffer (for the Ms-SNuPE reaction); and radioactive nucleotides. Additionally, bisulfite conversion reagents may include: DNA denaturation buffer; sulfonation buffer; DNA recovery regents or kit (e.g., precipitation, ultrafiltration, affinity column); desulfonation buffer; and DNA recovery components.
    • 5.3.3. Differential Binding-based Methylation Detection Methods
  • For identification of differentially methylated regions, one approach is to capture methylated DNA. This approach uses a protein, in which the methyl binding domain of MBD2 is fused to the Fc fragment of an antibody (MBD-FC) (Gebhard et al., 2006, Cancer Res. 66:6118-6128; and PCT Pub. No. WO 2006/056480 A2 (Relhi), the contents of which are hereby incorporated by reference in their entirety). This fusion protein has several advantages over conventional methylation specific antibodies. The MBD FC has a higher affinity to methylated DNA and it binds double stranded DNA. Most importantly the two proteins differ in the way they bind DNA. Methylation specific antibodies bind DNA stochastically, which means that only a binary answer can be obtained. The methyl binding domain of MBD-FC, on the other hand, binds DNA molecules regardless of their methylation status. The strength of this protein—DNA interaction is defined by the level of DNA methylation. After binding genomic DNA, eluate solutions of increasing salt concentrations can be used to fractionate non-methylated and methylated DNA allowing for a more controlled separation (Gebhard et al., 2006, Nucleic Acids Res. 34 e82). Consequently this method, called Methyl-CpG immunoprecipitation (MCIP), not only enriches, but also fractionates genomic DNA according to methylation level, which is particularly helpful when the unmethylated DNA fraction should be investigated as well.
  • Alternatively, one may use 5-methyl cytidine antibodies to bind and precipitate methylated DNA. Antibodies are available from Abcam (Cambridge, Mass.), Diagenode (Sparta, N.J.) or Eurogentec (c/o AnaSpec, Fremont, Calif.). Once the methylated fragments have been separated they may be sequenced using microarray based techniques such as methylated CpG-island recovery assay (MIRA) or methylated DNA immunoprecipitation (MeDIP) (Pelizzola et al., 2008, Genome Res. 18, 1652-1659; 0′ Geen et al., 2006, BioTechniques 41(5), 577-580, Weber et al., 2005, Nat. Genet. 37, 853-862; Horak and Snyder, 2002, Methods Enzymol., 350, 469-83; Lieb, 2003, Methods Mol. Biol., 224, 99-109). Another technique is methyl-CpG binding domain column/segregation of partly melted molecules (MBD/SPM, Shiraishi et al., 1999, Proc. Natl. Acad. Sci. USA 96(6):2913-2918).
    • 5.3.4. Methylation Specific Restriction Enzymatic Methods
  • For example, there are methyl-sensitive enzymes that preferentially or substantially cleave or digest at their DNA recognition sequence if it is non-methylated. Thus, an unmethylated DNA sample will be cut into smaller fragments than a methylated DNA sample. Similarly, a hypermethylated DNA sample will not be cleaved. In contrast, there are methyl-sensitive enzymes that cleave at their DNA recognition sequence only if it is methylated. Methyl-sensitive enzymes that digest unmethylated DNA suitable for use in methods of the technology include, but are not limited to, Hpall, Hhal, Maell, BstUI and Acil. An enzyme that can be used is Hpall that cuts only the unmethylated sequence CCGG. Another enzyme that can be used is Hhal that cuts only the unmethylated sequence GCGC. Both enzymes are available from New England BioLabs®, Inc. Combinations of two or more methyl-sensitive enzymes that digest only unmethylated DNA can also be used. Suitable enzymes that digest only methylated DNA include, but are not limited to, Dpnl, which only cuts at fully methylated 5′-GATC sequences, and McrBC, an endonuclease, which cuts DNA containing modified cytosines (5-methylcytosine or 5-hydroxymethylcytosine or N4-methylcytosine) and cuts at recognition site 5′ . . . PumC(N40-3000) PumC . . . 3′ (New England BioLabs, Inc., Beverly, Mass.). Cleavage methods and procedures for selected restriction enzymes for cutting DNA at specific sites are well known to the skilled artisan. For example, many suppliers of restriction enzymes provide information on conditions and types of DNA sequences cut by specific restriction enzymes, including New England BioLabs, Pro-Mega Biochems, Boehringer-Mannheim, and the like. Sambrook et al. (See Sambrook et al. Molecular Biology: A Laboratory Approach, Cold Spring Harbor, N. Y. 1989) provide a general description of methods for using restriction enzymes and other enzymes.
  • The MCA technique is a method that can be used to screen for altered methylation patterns in genomic DNA, and to isolate specific sequences associated with these changes (Toyota et al., 1999, Cancer Res. 59, 2307-2312, U.S. Pat. No. 7,700,324 (Issa et al.) the contents of which are hereby incorporated by reference in their entirety). Briefly, restriction enzymes with different sensitivities to cytosine methylation in their recognition sites are used to digest genomic DNAs from primary tumors, cell lines, and normal tissues prior to arbitrarily primed PCR amplification. Fragments that show differential methylation are cloned and sequenced after resolving the PCR products on high-resolution polyacrylamide gels. The cloned fragments are then used as probes for Southern analysis to confirm differential methylation of these regions. Typical reagents (e.g., as might be found in a typical MCA-based kit) for MCA analysis may include, but are not limited to: PCR primers for arbitrary priming Genomic DNA; PCR buffers and nucleotides, restriction enzymes and appropriate buffers; gene-hybridization oligos or probes; control hybridization oligos or probes.
    • 5.3.5. Methylation-Sensitive High Resolution Melting (HRM)
  • Recently, Wojdacz et al. reported methylation-sensitive high resolution melting as a technique to assess methylation. (Wojdacz and Dobrovic, 2007, Nuc. Acids Res. 35(6) e41; Wojdacz et al. 2008, Nat. Prot. 3(12) 1903-1908; Balic et al., 2009 J. Mol. Diagn. 11 102-108; and US Pat. Pub. No. 2009/0155791 (Wojdacz et al.), the contents of which are hereby incorporated by reference in their entirety). A variety of commercially available real time PCR machines have HRM systems including the Roche LightCycler480, Corbett Research RotorGene6000, and the Applied Biosystems 7500. HRM may also be combined with other amplification techniques such as pyrosequencing as described by Candiloro et al. (Candiloro et al., 2011, Epigenetics 6(4) 500-507). Any of SEQ ID NO 1-353, or portions thereof, may be used in a HRM assay.
    • 5.3.6. Mass Spectroscopic Detection Methods
  • Another method for analyzing methylation sites is a primer extension assay, including an optimized PCR amplification reaction that produces amplified targets for analysis using mass spectrometry. The assay can also be done in multiplex. Mass spectrometry is a particularly effective method for the detection of polynucleotides associated with the differentially methylated regulatory elements. The presence of the polynucleotide sequence is verified by comparing the mass of the detected signal with the expected mass of the polynucleotide of interest. The relative signal strength, e.g., mass peak on a spectra, for a particular polynucleotide sequence indicates the relative population of a specific allele, thus enabling calculation of the allele ratio directly from the data. This method is described in detail in PCT Pub. No. WO 2005/012578A1 (Beaulieu et al.) which is hereby incorporated by reference in its entirety. For methylation analysis, the assay can be adopted to detect bisulfite introduced methylation dependent C to T sequence changes. These methods are particularly useful for performing multiplexed amplification reactions and multiplexed primer extension reactions (e g., multiplexed homogeneous primer mass extension (hME) assays) in a single well to further increase the throughput and reduce the cost per reaction for primer extension reactions.
  • For a review of mass spectrometry methods using Sequenom® standard iPLEX™ assay and MassARRAY® technology, see Jurinke et al., 2004, Mol. Biotechnol. 26, 147-164. For methods of detecting and quantifying target nucleic acids using cleavable detector probes that are cleaved during the amplification process and detected by mass spectrometry, see PCT Pub. Nos. WO 2006/031745 (Van Der Boom and Boecker); WO 2009/073251 A1(Van Den Boom et al.); WO 2009/114543 A2 (Oeth et al.); and WO 2010/033639 A2 (Ehrich et al.); which are hereby incorporated by reference in their entirety.
    • 5.3.7. Additional Methods for Methylation Analysis
  • Other methods for DNA methylation analysis include restriction landmark genomic scanning (RLGS, Costello et al., 2002, Meth. Mol. Biol., 200, 53-70), methylation-sensitive-representational difference analysis (MS-RDA, Ushijima and Yamashita, 2009, Methods Mol Biol. 507, 117-130). Comprehensive high-throughput arrays for relative methylation (CHARM) techniques are described in WO 2009/021141 (Feinberg and Irizarry). The Roche® NimbleGen® microarrays including the Chromatin Immunoprecipitation-on-chip (ChIP-chip) or methylated DNA immunoprecipitation-on-chip (MeDIP-chip). These tools have been used for a variety of cancer applications including melanoma, liver cancer and lung cancer (Koga et al., 2009, Genome Res., 19, 1462-1470; Acevedo et al., 2008, Cancer Res., 68, 2641-2651; Rauch et al., 2008, Proc. Nat. Acad. Sci. USA, 105, 252-257). Others have reported bisulfate conversion, padlock probe hybridization, circularization, amplification and next generation or multiplexed sequencing for high throughput detection of methylation (Deng et al., 2009, Nat. Biotechnol. 27, 353-360; Ball et al., 2009, Nat. Biotechnol. 27, 361-368; U.S. Pat. No. 7,611,869 (Fan)). As an alternative to bisulfate oxidation, Bayeyt et al. have reported selective oxidants that oxidize 5-methylcytosine, without reacting with thymidine, which are followed by PCR or pyrosequencing (WO 2009/049916 (Bayeyt et al.). These references for these techniques are hereby incorporated by reference in their entirety.
    • 5.3.8. Polynucleotide Sequence Amplification and Determination
  • Following reaction or separation of nucleic acid in a methylation specific manner, the nucleic acid may be subjected to sequence-based analysis. Furthermore, once it is determined that one particular melanoma genomic sequence is hypermethylated or hypomethylated compared to the benign counterpart, the amount of this genomic sequence can be determined. Subsequently, this amount can be compared to a standard control value and serve as an indication for the melanoma. In many instances, it is desirable to amplify a nucleic acid sequence using any of several nucleic acid amplification procedures which are well known in the art. Specifically, nucleic acid amplification is the chemical or enzymatic synthesis of nucleic acid copies which contain a sequence that is complementary to a nucleic acid sequence being amplified (template). The methods and kits of the invention may use any nucleic acid amplification or detection methods known to one skilled in the art, such as those described in U.S. Pat. No. 5,525,462 (Takarada et al.); U.S. Pat. No. 6,114,117 (Hepp et al.); U.S. Pat. No. 6,127,120 (Graham et al.); U.S. Pat. No. 6,344,317 (Urnovitz); U.S. Pat. No. 6,448,001 (Oku); U.S. Pat. No. 6,528,632 (Catanzariti et al.); and PCT Pub. No. WO 2005/111209 (Nakajima et al.); all of which are incorporated herein by reference in their entirety.
  • In some embodiments, the nucleic acids are amplified by PCR amplification using methodologies known to one skilled in the art. One skilled in the art will recognize, however, that amplification can be accomplished by any known method, such as ligase chain reaction (LCR), Qβ-replicase amplification, rolling circle amplification, transcription amplification, self-sustained sequence replication, nucleic acid sequence-based amplification (NASBA), each of which provides sufficient amplification. Branched-DNA technology may also be used to qualitatively demonstrate the presence of a sequence of the technology, which represents a particular methylation pattern, or to quantitatively determine the amount of this particular genomic sequence in a sample. Nolte reviews branched-DNA signal amplification for direct quantitation of nucleic acid sequences in clinical samples (Nolte, 1998, Adv. Clin. Chem. 33:201-235).
  • The PCR process is well known in the art and is thus not described in detail herein. For a review of PCR methods and protocols, see, e.g., Innis et al., eds., PCR Protocols, A Guide to Methods and Application, Academic Press, Inc., San Diego, Calif. 1990; U.S. Pat. No. 4,683,202 (Mullis); which are incorporated herein by reference in their entirety. PCR reagents and protocols are also available from commercial vendors, such as Roche Molecular Systems. PCR may be carried out as an automated process with a thermostable enzyme. In this process, the temperature of the reaction mixture is cycled through a denaturing region, a primer annealing region, and an extension reaction region automatically. Machines specifically adapted for this purpose are commercially available.
  • Amplified sequences may also be measured using invasive cleavage reactions such as the Invader® technology (Zou et al., 2010, Association of Clinical Chemistry (AACC) poster presentation on Jul. 28, 2010, “Sensitive Quantification of Methylated Markers with a Novel Methylation Specific Technology,” available at www.exactsciences.com; and U.S. Pat. No. 7,011,944 (Prudent et al.) which are incorporated herein by reference in their entirety).
    • 5.3.9. High Throughput and Single Molecule Sequencing Technology
  • Suitable next generation sequencing technologies are widely available. Examples include the 454 Life Sciences platform (Roche, Branford, Conn.) (Margulies et al. 2005 Nature, 437, 376-380); Illumina's Genome Analyzer, GoldenGate Methylation Assay, or Infinium Methylation Assays, i.e., Infinium HumanMethylation 27K BeadArray or VeraCode GoldenGate methylation array (Illumina, San Diego, Calif.; Bibkova et al., 2006, Genome Res. 16, 383-393; U.S. Pat. Nos. 6,306,597 and 7,598,035 (Macevicz); U.S. Pat. No. 7,232,656 (Balasubramanian et al.)); or DNA Sequencing by Ligation, SOLiD System (Applied Biosystems/Life Technologies; U.S. Pat. Nos. 6,797,470, 7,083,917, 7,166,434, 7,320,865, 7,332,285, 7,364,858, and 7,429,453 (Barany et al.); or the Helicos True Single Molecule DNA sequencing technology (Harris et al., 2008 Science, 320, 106-109; U.S. Pat. Nos. 7,037,687 and 7,645,596 (Williams et al.); U.S. Pat. No. 7,169,560 (Lapidus et al.); U.S. Pat. No. 7,769,400 (Harris)), the single molecule, real-time (SMRT™) technology of Pacific Biosciences, and sequencing (Soni and Meller, 2007, Clin. Chem. 53, 1996-2001) which are incorporated herein by reference in their entirety. These systems allow the sequencing of many nucleic acid molecules isolated from a specimen at high orders of multiplexing in a parallel fashion (Dear, 2003, Brief Funct. Genomic Proteomic, 1(4), 397-416 and McCaughan and Dear, 2010, J. Pathol., 220, 297-306). Each of these platforms allow sequencing of clonally expanded or non-amplified single molecules of nucleic acid fragments. Certain platforms involve, for example, (i) sequencing by ligation of dye-modified probes (including cyclic ligation and cleavage), (ii) pyrosequencing, and (iii) single-molecule sequencing.
  • Pyrosequencing is a nucleic acid sequencing method based on sequencing by synthesis, which relies on detection of a pyrophosphate released on nucleotide incorporation. Generally, sequencing by synthesis involves synthesizing, one nucleotide at a time, a DNA strand complimentary to the strand whose sequence is being sought. Study nucleic acids may be immobilized to a solid support, hybridized with a sequencing primer, incubated with DNA polymerase, ATP sulfurylase, luciferase, apyrase, adenosine 5′ phosphsulfate and luciferin. Nucleotide solutions are sequentially added and removed. Correct incorporation of a nucleotide releases a pyrophosphate, which interacts with ATP sulfurylase and produces ATP in the presence of adenosine 5′ phosphsulfate, fueling the luciferin reaction, which produces a chemiluminescent signal allowing sequence determination. Machines for pyrosequencing and methylation specific reagents are available from Qiagen, Inc. (Valencia, Calif.). See also Tost and Gut, 2007, Nat. Prot. 2 2265-2275. An example of a system that can be used by a person of ordinary skill based on pyrosequencing generally involves the following steps: ligating an adaptor nucleic acid to a study nucleic acid and hybridizing the study nucleic acid to a bead; amplifying a nucleotide sequence in the study nucleic acid in an emulsion; sorting beads using a picoliter multiwell solid support; and sequencing amplified nucleotide sequences by pyrosequencing methodology (e.g., Nakano et al., 2003, J. Biotech. 102, 117-124). Such a system can be used to exponentially amplify amplification products generated by a process described herein, e.g., by ligating a heterologous nucleic acid to the first amplification product generated by a process described herein.
  • Certain single-molecule sequencing embodiments are based on the principal of sequencing by synthesis, and utilize single-pair Fluorescence Resonance Energy Transfer (single pair FRET) as a mechanism by which photons are emitted as a result of successful nucleotide incorporation. The emitted photons often are detected using intensified or high sensitivity cooled charge-couple-devices in conjunction with total internal reflection microscopy (TIRM). Photons are only emitted when the introduced reaction solution contains the correct nucleotide for incorporation into the growing nucleic acid chain that is synthesized as a result of the sequencing process. In FRET based single-molecule sequencing or detection, energy is transferred between two fluorescent dyes, sometimes polymethine cyanine dyes Cy3 and Cy5, through long-range dipole interactions. The donor is excited at its specific excitation wavelength and the excited state energy is transferred, non-radiatively to the acceptor dye, which in turn becomes excited. The acceptor dye eventually returns to the ground state by radiative emission of a photon. The two dyes used in the energy transfer process represent the “single pair”, in single pair FRET. Cy3 often is used as the donor fluorophore and often is incorporated as the first labeled nucleotide. Cy5 often is used as the acceptor fluorophore and is used as the nucleotide label for successive nucleotide additions after incorporation of a first Cy3 labeled nucleotide. The fluorophores generally are within 10 nanometers of each other for energy transfer to occur successfully. Bailey et al. recently reported a highly sensitive (15 pg methylated DNA) method using quantum dots to detect methylation status using fluorescence resonance energy transfer (MS-qFRET)(Bailey et al. 2009, Genome Res. 19(8), 1455-1461, which is incorporated herein by reference in its entirety).
  • An example of a system that can be used based on single-molecule sequencing generally involves hybridizing a primer to a study nucleic acid to generate a complex; associating the complex with a solid phase; iteratively extending the primer by a nucleotide tagged with a fluorescent molecule; and capturing an image of fluorescence resonance energy transfer signals after each iteration (e.g., Braslaysky et al., PNAS 100(7): 3960-3964 (2003); U.S. Pat. No. 7,297,518 (Quake et al.) which are incorporated herein by reference in their entirety). Such a system can be used to directly sequence amplification products generated by processes described herein. In some embodiments the released linear amplification product can be hybridized to a primer that contains sequences complementary to immobilized capture sequences present on a solid support, a bead or glass slide for example. Hybridization of the primer-released linear amplification product complexes with the immobilized capture sequences, immobilizes released linear amplification products to solid supports for single pair FRET based sequencing by synthesis. The primer often is fluorescent, so that an initial reference image of the surface of the slide with immobilized nucleic acids can be generated. The initial reference image is useful for determining locations at which true nucleotide incorporation is occurring. Fluorescence signals detected in array locations not initially identified in the “primer only” reference image are discarded as non-specific fluorescence. Following immobilization of the primer-released linear amplification product complexes, the bound nucleic acids often are sequenced in parallel by the iterative steps of, a) polymerase extension in the presence of one fluorescently labeled nucleotide, b) detection of fluorescence using appropriate microscopy, TIRM for example, c) removal of fluorescent nucleotide, and d) return to step a with a different fluorescently labeled nucleotide.
  • The technology may be practiced with digital PCR. Digital PCR was developed by Kalinina and colleagues (Kalinina et al., 1997, Nucleic Acids Res. 25; 1999-2004) and further developed by Vogelstein and Kinzler (1999, Proc. Natl. Acad. Sci. U.S.A. 96; 9236-9241). The application of digital PCR is described by Cantor et al. (PCT Pub. Nos. WO 2005/023091A2 (Cantor et al.); WO 2007/092473 A2, (Quake et al.)), which are hereby incorporated by reference in their entirety. Digital PCR takes advantage of nucleic acid (DNA, cDNA or RNA) amplification on a single molecule level, and offers a highly sensitive method for quantifying low copy number nucleic acid. Fluidigm® Corporation offers systems for the digital analysis of nucleic acids.
  • In some embodiments, nucleotide sequencing may be by solid phase single nucleotide sequencing methods and processes. Solid phase single nucleotide sequencing methods involve contacting sample nucleic acid and solid support under conditions in which a single molecule of sample nucleic acid hybridizes to a single molecule of a solid support. Such conditions can include providing the solid support molecules and a single molecule of sample nucleic acid in a “microreactor.” Such conditions also can include providing a mixture in which the sample nucleic acid molecule can hybridize to solid phase nucleic acid on the solid support. Single nucleotide sequencing methods useful in the embodiments described herein are described in PCT Pub. No. WO 2009/091934 (Cantor).
  • In certain embodiments, nanopore sequencing detection methods include (a) contacting a nucleic acid for sequencing (“base nucleic acid,” e.g., linked probe molecule) with sequence-specific detectors, under conditions in which the detectors specifically hybridize to substantially complementary subsequences of the base nucleic acid; (b) detecting signals from the detectors and (c) determining the sequence of the base nucleic acid according to the signals detected. In certain embodiments, the detectors hybridized to the base nucleic acid are disassociated from the base nucleic acid (e.g., sequentially dissociated) when the detectors interfere with a nanopore structure as the base nucleic acid passes through a pore, and the detectors disassociated from the base sequence are detected.
  • A detector also may include one or more regions of nucleotides that do not hybridize to the base nucleic acid. In some embodiments, a detector is a molecular beacon. A detector often comprises one or more detectable labels independently selected from those described herein. Each detectable label can be detected by any convenient detection process capable of detecting a signal generated by each label (e.g., magnetic, electric, chemical, optical and the like). For example, a CD camera can be used to detect signals from one or more distinguishable quantum dots linked to a detector.
  • The invention encompasses any method known in the art for enhancing the sensitivity of the detectable signal in such assays, including, but not limited to, the use of cyclic probe technology (Bakkaoui et al., 1996, BioTechniques 20: 240-8, which is incorporated herein by reference in its entirety); and the use of branched probes (Urdea et al., 1993, Clin. Chem. 39, 725-6; which is incorporated herein by reference in its entirety). The hybridization complexes are detected according to well-known techniques in the art.
  • Reverse transcribed or amplified nucleic acids may be modified nucleic acids. Modified nucleic acids can include nucleotide analogs, and in certain embodiments include a detectable label and/or a capture agent. Examples of detectable labels include, without limitation, fluorophores, radioisotopes, colorimetric agents, light emitting agents, chemiluminescent agents, light scattering agents, enzymes and the like. Examples of capture agents include, without limitation, an agent from a binding pair selected from antibody/antigen, antibody/antibody, antibody/antibody fragment, antibody/antibody receptor, antibody/protein A or protein G, hapten/anti-hapten, biotin/avidin, biotin/streptavidin, folic acid/folate binding protein, vitamin B 12/intrinsic factor, chemical reactive group/complementary chemical reactive group (e.g., sulfhydryl/maleimide, sulfhydryl/haloacetyl derivative, amine/isotriocyanate, amine/succinimidyl ester, and amine/sulfonyl halides) pairs, and the like. Modified nucleic acids having a capture agent can be immobilized to a solid support in certain embodiments.
    • 5.4. Additional Methods 5.4.1. Antibody Staining/Detection
  • In some embodiments, the invention may encompass detecting and/or quantitating using antibodies either alone or in conjunction with measurement of methylation levels. Antibodies are already used in current practice in the classification and/or diagnosis of melanocytic lesions (Alonso et al., 2004, Am. J. Pathol. 164(1) 193-203; Ivan & Prieto, 2010, Future Oncol. 6(7), 1163-1175; Linos et al., 2011, Biomarkers Med. 5(3) 333-360; and Rothberg et al., 2009 J. Nat. Canc. Inst. 101(7) 452-474, the contents of which are hereby incorporated by reference in their entireties). Examples of antibodies that are used include HMB45/gp100 (Abcam; AbD Serotec; BioGenex, San Ramon, Calif.; Biocare Medical, Concord, Calif.); MART-1/Melan-A (Abcam; AbD Serotec; BioGenex; Thermo Scientific Pierce Abs., Rockford, Ill.); Microphthalmia transcription factor/MITF-1 (Invitrogen); NKI/C3 (Melanoma Associated Antigen 100+/7 kDa)(Abcam; Thermo Scientific Pierce Abs.); p75NTR/neurotrophin receptor (Abcam; AbD Serotec; Promega, Madison, Wis.); S100 (Abcam; AbD Serotec, Raleigh, N.C.; BioGenex); Tyrosinase (Abcam; AbD Serotec; Thermo Scientific Pierce Abs.). In one embodiment a cocktail of 5100, HMB-45 and MART-1/Melan-A is used. Antibodies may also be used to detect the gene products of the methylated genes described herein. Specifically, genes hypomethylated would be expected to show over-expression and genes hypermethylated would be expected to show under-expression. Staining markers of tumor vascular formation may also be used in conjunction with the present invention (Bhati et al., 2008, Am. J. Pathol. 172(5), 1381-1390, including Table 1 on page 1387, the contents of which are incorporated herein by reference in their entirety).
  • Antibody reagents can be used in assays to detect expression levels of in patient samples using any of a number of immunoassays known to those skilled in the art. Immunoassay techniques and protocols are generally described in Price and Newman, “Principles and Practice of Immunoassay,” 2nd Edition, Grove's Dictionaries, 1997; and Gosling, “Immunoassays: A Practical Approach,” Oxford University Press, 2000. A variety of immunoassay techniques, including competitive and non-competitive immunoassays, can be used. See, e.g., Self et al., 1996, Curr. Opin. Biotechnol., 7, 60-65. The term immunoassay encompasses techniques including, without limitation, enzyme immunoassays (EIA) such as enzyme multiplied immunoassay technique (EMIT), enzyme-linked immunosorbent assay (ELISA), IgM antibody capture ELISA (MAC ELISA), and microparticle enzyme immunoassay (MEIA); capillary electrophoresis immunoassays (CEIA); radioimmunoassays (RIA); immunoradiometric assays (IRMA); fluorescence polarization immunoassays (FPIA); and chemiluminescence assays (CL). If desired, such immunoassays can be automated. Immunoassays can also be used in conjunction with laser induced fluorescence. See, e.g., Schmalzing et al., 1997, Electrophoresis, 18, 2184-2193; Bao, 1997, J. Chromatogr. B. Biomed. Sci., 699, 463-480. Liposome immunoassays, such as flow-injection liposome immunoassays and liposome immunosensors, are also suitable for use in the present invention. See, e.g., Rongen et al., 1997, J. Immunol. Methods, 204, 105-133. In addition, nephelometry assays, in which the formation of protein/antibody complexes results in increased light scatter that is converted to a peak rate signal as a function of the marker concentration, are suitable for use in the methods of the present invention. Nephelometry assays are commercially available from Beckman Coulter (Brea, Calif.) and can be performed using a Behring Nephelometer Analyzer (Fink et al., 1989, J. Clin. Chem. Clin. Biochem., 27, 261-276).
  • Specific immunological binding of the antibody to nucleic acids can be detected directly or indirectly. Direct labels include fluorescent or luminescent tags, metals, dyes, radionuclides, and the like, attached to the antibody. An antibody labeled with iodine—125 125I can be used. A chemiluminescence assay using a chemiluminescent antibody specific for the nucleic acid is suitable for sensitive, non-radioactive detection of protein levels. An antibody labeled with fluorochrome is also suitable. Examples of fluorochromes include, without limitation, DAPI, fluorescein, Hoechst 33258, R-phycocyanin, B-phycoerythrin, R-phycoerythrin, rhodamine, Texas red, and lissamine. Indirect labels include various enzymes well known in the art, such as horseradish peroxidase (HRP), alkaline phosphatase (AP), β-galactosidase, urease, and the like. A horseradish-peroxidase detection system can be used, for example, with the chromogenic substrate tetramethylbenzidine (TMB), which yields a soluble product in the presence of hydrogen peroxide that is detectable at 450 nm. An alkaline phosphatase detection system can be used with the chromogenic substrate p-nitrophenyl phosphate, for example, which yields a soluble product readily detectable at 405 nm. Similarly, a β-galactosidase detection system can be used with the chromogenic substrate o-nitrophenyl-β-D-galactopyranoside (ONPG), which yields a soluble product detectable at 410 nm An urease detection system can be used with a substrate such as urea-bromocresol purple (Sigma Immunochemicals; St. Louis, Mo.).
  • A signal from the direct or indirect label can be analyzed, for example, using a spectrophotometer to detect color from a chromogenic substrate; a radiation counter to detect radiation such as a gamma counter for detection of 125I; or a fluorometer to detect fluorescence in the presence of light of a certain wavelength. For detection of enzyme-linked antibodies, a quantitative analysis can be made using a spectrophotometer such as an EMAX Microplate Reader (Molecular Devices; Menlo Park, Calif.) in accordance with the manufacturer's instructions. If desired, the assays of the present invention can be automated or performed robotically, and the signal from multiple samples can be detected simultaneously.
  • The antibodies can be immobilized onto a variety of solid supports, such as magnetic or chromatographic matrix particles, the surface of an assay plate (e.g., microtiter wells), pieces of a solid substrate material or membrane (e.g., plastic, nylon, paper), and the like. An assay strip can be prepared by coating the antibody or a plurality of antibodies in an array on a solid support. This strip can then be dipped into the test sample and processed quickly through washes and detection steps to generate a measurable signal, such as a colored spot. The antibodies may be in an array one or more antibodies, single or double stranded nucleic acids, proteins, peptides or fragments thereof, amino acid probes, or phage display libraries. Many protein/antibody arrays are described in the art. These include, for example, arrays produced by Ciphergen Biosystems (Fremont, Calif.), Packard BioScience Company (Meriden Conn.), Zyomyx (Hayward, Calif.) and Phylos (Lexington, Mass.). Examples of such arrays are described in the following patents: U.S. Pat. No. 6,225,047 (Hutchens and Yip); U.S. Pat. No. 6,537,749 (Kuimelis and Wagner); and U.S. Pat. No. 6,329,209 (Wagner et al.), all of which are incorporated herein by reference in their entirety.
    • 5.4.2. Fluorescence in situ Hybridization (FISH) and Comparative Genomic Hybridization (CGH)
  • In some embodiments, the invention may further encompass detecting and/or quantitating using fluorescence in situ hybridization (FISH) in a sample, preferably a tissue sample, obtained from a subject in accordance with the methods of the invention. FISH is a common methodology used in the art, especially in the detection of specific chromosomal aberrations in tumor cells, for example, to aid in diagnosis and tumor staging. As applied in the methods of the invention, it can be used in conjunction with detecting methylation. For reviews of FISH methodology, see, e.g., Weier et al., 2002, Expert Rev. Mol. Diagn. 2 (2): 109-119; Trask et al., 1991, Trends Genet. 7 (5): 149-154; and Tkachuk et al., 1991, Genet. Anal. Tech. Appl. 8: 676-74; U.S. Pat. No. 6,174,681 (Halling et al.); for multi-color FISH specific to melanoma, see Gerami et al., 2009, Am. J. Surg. Pathol. 33(8) 1146-1156; and PCT Pub. No. WO 2007/028031 A2 (Bastian et al.); all of which are incorporated herein by reference in their entirety. Alternatively, comparative genomic hybridization (CGH) also may be used as part of the methods disclosed herein. Specifically, Bastian et al. describe CGH as a means to find patterns of chromosomal aberrations associated with melanoma (Bastian et al., 2003, Am. J. Pathol. 163(5) 1765-1770).
  • In alternative embodiments, the invention encompasses use of additional melanoma specific gene expression and/or antibody assays either in situ, i.e., directly upon tissue sections (fixed and/or frozen) of patient tissue obtained from biopsies or resections, such that no nucleic acid purification is necessary; or based on extracted and/or amplified nucleic acids. Targets for such assays are disclosed in Haqq et al. 2005, Proc. Nat. Acad. Sci. USA, 102(17), 6092-6097; Riker et al., 2008, BMC Med. Genomics, 1, 13, pub. 28 Apr. 2008; Hoek et al., 2004, Can. Res. 64, 5270-5282; PCT Pub. Nos. WO 2008/030986 and WO 2009/111661(Kashani-Sabet & Haqq); U.S. Pat. No. 7,247,426 (Yakhini et al.), all of which are incorporated herein by reference in their entirety. Several researchers have reported the use of microRNAs (miRNA) for cancer or melanoma detection. These methods could be used in combination with the methylation methods described herein (see Mueller et al., 2009, J. Invest. Dermatol., 129, 1740-1751; Leidinger et al., 2010, BMC Cancer, 10, 262; U.S. Pat. Pub. 2009/0220969 (Chiang and Shi); PCT Pub. No. WO 2010/068473 (Reynolds and Siva); which are hereby incorporated by reference in their entirety). Alternatively, the methylated nucleic acids may be detected in blood either as free DNA or in circulating tumor cells. For in situ procedures see, e.g., Nuovo, G. J., 1992, PCR In Situ Hybridization: Protocols And Applications, Raven Press, NY, which is incorporated herein by reference in its entirety.
  • Methods for making nucleic acid microarrays are known to the skilled artisan and are described, for example, in Lockhart et al., 1996, Nat. Biotech. 14,1675-1680, 1996 Schena et al., 1996, Proc. Natl. Acad. Sci. USA, 93, 10614-10619, U.S. Pat. No. 5,837,832 (Chee et al.) and PCT Pub. No. WO 00/56934 (Englert et al.), herein incorporated by reference. To produce a nucleic acid microarray, oligonucleotides may be synthesized or bound to the surface of a substrate using a chemical coupling procedure and an ink jet application apparatus, as described U.S. Pat. No. 6,015,880 (Baldeschweiler et al.), incorporated herein by reference. Alternatively, a gridded array may be used to arrange and link cDNA fragments or oligonucleotides to the surface of a substrate using a vacuum system, thermal, UV, mechanical or chemical bonding procedure.
  • The measurement of differentially methylated elements associated with melanoma may alone, or in conjunction with other melanoma detection tools discussed above (antibody staining, PCR, CGH, FISH) may have several other non-limiting uses. Amongst these uses are: (i) reclassifying specimens that were indeterminate or difficult to identify in a pathology laboratory; (ii) deciding to follow up with a lymph node examination and/or PET/CAT/MRI or other imaging methods; (iii) determining the frequency of follow up visits; or (iv) initiating other investigatory analysis such as a blood draw and evaluation for circulating tumor cells. Furthermore, the differentially methylated elements associated with melanoma may help to determine which patients would benefit from adjuvant treatment after surgical resection.
    • 5.5. Compositions and Kits
  • The invention provides compositions and kits measuring methylation or polypeptides or polynucleotides regulated by the differentially methylated elements described herein using DNA methylation specific assays, antibodies specific for the polypeptides or nucleic acids specific for the polynucleotides. Kits for carrying out the diagnostic assays of the invention typically include, in suitable container means, (i) a reagent for methylation specific reaction or separation, (ii) a probe that comprises an antibody or nucleic acid sequence that specifically binds to the marker polypeptides or polynucleotides of the invention, (iii) a label for detecting the presence of the probe and (iv) instructions for how to measure the level of methylation (or polypeptide or polynucleotide). The kits may include several antibodies or polynucleotide sequences encoding polypeptides of the invention, e.g., a first antibody and/or second and/or third and/or additional antibodies that recognize a protein encoded by a gene differentially methylated in melanoma. The container means of the kits will generally include at least one vial, test tube, flask, bottle, syringe and/or other container into which a first antibody specific for one of the polypeptides or a first nucleic acid specific for one of the polynucleotides of the present invention may be placed and/or suitably aliquoted. Where a second and/or third and/or additional component is provided, the kit will also generally contain a second, third and/or other additional container into which this component may be placed. Alternatively, a container may contain a mixture of more than one antibody or nucleic acid reagent, each reagent specifically binding a different marker in accordance with the present invention. The kits of the present invention will also typically include means for containing the antibody or nucleic acid probes in close confinement for commercial sale. Such containers may include injection and/or blow-molded plastic containers into which the desired vials are retained.
  • The kits may further comprise positive and negative controls, as well as instructions for the use of kit components contained therein, in accordance with the methods of the present invention.
    • 5.6. In Vivo Imaging
  • The various markers of the invention also provide reagents for in vivo imaging such as, for instance, the imaging of metastasis of melanoma to regional lymph nodes using labeled reagents that detect (i) DNA methylation associated with melanoma, (ii) a polypeptide or polynucleotide regulated by the differentially methylated elements. In vivo imaging techniques may be used, for example, as guides for surgical resection or to detect the distant spread of melanoma. For in vivo imaging purposes, reagents that detect the presence of these proteins or genes, such as antibodies, may be labeled with a positron-emitting isotope (e.g., 18 F) for positron emission tomography (PET), gamma-ray isotope (e.g., 99mTc) for single photon emission computed tomography (SPECT), a paramagnetic molecule or nanoparticle (e.g., Gd3+ chelate or coated magnetite nanoparticle) for magnetic resonance imaging (MRI), a near-infrared fluorophore for near-infra red (near-IR) imaging, a luciferase (firefly, bacterial, or coelenterate), green fluorescent protein, or other luminescent molecule for bioluminescence imaging, or a perfluorocarbon-filled vesicle for ultrasound. Fluorodeoxyglucose (FDG)-PET metabolic uptake alone or in combination with MRI is particularly useful.
  • Furthermore, such reagents may include a fluorescent moiety, such as a fluorescent protein, peptide, or fluorescent dye molecule. Common classes of fluorescent dyes include, but are not limited to, xanthenes such as rhodamines, rhodols and fluoresceins, and their derivatives; bimanes; coumarins and their derivatives such as umbelliferone and aminomethyl coumarins; aromatic amines such as dansyl; squarate dyes; benzofurans; fluorescent cyanines; carbazoles; dicyanomethylene pyranes, polymethine, oxabenzanthrane, xanthene, pyrylium, carbostyl, perylene, acridone, quinacridone, rubrene, anthracene, coronene, phenanthrecene, pyrene, butadiene, stilbene, lanthanide metal chelate complexes, rare-earth metal chelate complexes, and derivatives of such dyes. Fluorescent dyes are discussed, for example, in U.S. Pat. No. 4,452,720 (Harada et al.); U.S. Pat. No. 5,227,487 (Haugland and Whitaker); and U.S. Pat. No. 5,543,295 (Bronstein et al.). Other fluorescent labels suitable for use in the practice of this invention include a fluorescein dye. Typical fluorescein dyes include, but are not limited to, 5-carboxyfluorescein, fluorescein-5-isothiocyanate and 6-carboxyfluorescein; examples of other fluorescein dyes can be found, for example, in U.S. Pat. No. 4,439,356 (Khanna and Colvin); U.S. Pat. No. 5,066,580 (Lee), U.S. Pat. No. 5,750,409 (Hermann et al.); and U.S. Pat. No. 6,008,379 (Benson et al.). The kits may include a rhodamine dye, such as, for example, tetramethylrhodamine-6-isothiocyanate, 5-carboxytetramethylrhodamine, 5-carboxy rhodol derivatives, tetramethyl and tetraethyl rhodamine, diphenyldimethyl and diphenyldiethyl rhodamine, dinaphthyl rhodamine, rhodamine 101 sulfonyl chloride (sold under the tradename of TEXAS RED®, and other rhodamine dyes. Other rhodamine dyes can be found, for example, in U.S. Pat. No. 5,936,087 (Benson et al.), U.S. Pat. No. 6,025,505 (Lee et al.); U.S. Pat. No. 6,080,852 (Lee et al.). The kits may include a cyanine dye, such as, for example, Cy3, Cy3B, Cy3.5, Cy5, Cy5.5, Cy7. Phosphorescent compounds including porphyrins, phthalocyanines, polyaromatic compounds such as pyrenes, anthracenes and acenaphthenes, and so forth, may also be used.
    • 5.7. Methods to Identify Compounds
  • A variety of methods may be used to identify compounds that modulate DNA methylation and prevent or treat melanoma progression. Typically, an assay that provides a readily measured parameter is adapted to be performed in the wells of multi-well plates in order to facilitate the screening of members of a library of test compounds as described herein. Thus, in one embodiment, an appropriate number of cells can be plated into the cells of a multi-well plate, and the effect of a test compound on the expression of a gene differentially methylated in melanoma can be determined. The compounds to be tested can be any small chemical compound, or a macromolecule, such as a protein, sugar, nucleic acid or lipid. Typically, test compounds will be small chemical molecules and peptides. Essentially any chemical compound can be used as a test compound in this aspect of the invention, although most often compounds that can be dissolved in aqueous or organic (especially DMSO-based) solutions are used. The assays are designed to screen large chemical libraries by automating the assay steps and providing compounds from any convenient source to assays, which are typically run in parallel (e.g., in microtiter formats on microtiter plates in robotic assays). It will be appreciated that there are many suppliers of chemical compounds, including Sigma (St. Louis, Mo.), Aldrich (St. Louis, Mo.), Sigma-Aldrich (St. Louis, Mo.), Fluka Chemika-Biochemica Analytika (Buchs Switzerland) and the like.
  • In one preferred embodiment, high throughput screening methods are used which involve providing a combinatorial chemical or peptide library containing a large number of potential therapeutic compounds. Such “combinatorial chemical libraries” or “ligand libraries” are then screened in one or more assays, as described herein, to identify those library members (particular chemical species or subclasses) that display a desired characteristic activity. In this instance, such compounds are screened for their ability to modulate the expression of gene differentially methylated in melanoma. A combinatorial chemical library is a collection of diverse chemical compounds generated by either chemical synthesis or biological synthesis, by combining a number of chemical “building blocks” such as reagents. For example, a linear combinatorial chemical library such as a polypeptide library is formed by combining a set of chemical building blocks (amino acids) in every possible way for a given compound length (i.e., the number of amino acids in a polypeptide compound). Millions of chemical compounds can be synthesized through such combinatorial mixing of chemical building blocks.
  • Preparation and screening of combinatorial chemical libraries are well known to those of skill in the art. Such combinatorial chemical libraries include, but are not limited to, peptide libraries (see, e.g., U.S. Pat. No. 5,010,175 (Rutter and Santi), Furka, 1991, Int. J. Pept. Prot. Res., 37:487-493; and Houghton et al., 1991, Nature, 354:84-88). Other chemistries for generating chemical diversity libraries can also be used. Such chemistries include, but are not limited to: U.S. Pat. No. 6,075,121 (Bartlett et al.) peptoids; U.S. Pat. No. 6,060,596 (Lerner et al.) encoded peptides; 5,858,670 (Lam et al.) random bio-oligomers; 5,288,514 (Ellman) benzodiazepines; 5,539,083 (Cook et al.) peptide nucleic acid libraries; 5,593,853 (Chen and Radmer) carbohydrate libraries; 5,569,588 (Ashby and Rine) isoprenoids; 5,549,974 (Holmes) thiazolidinones and metathiazanones; 5,525,735 (Takarada et al.) and 5,519,134 (Acevado and Hebert) pyrrolidines; 5,506,337 (Summerton and Weller) morpholino compounds; 5,288,514 (Ellman) benzodiazepines; diversomers such as hydantoins, benzodiazepines and dipeptides (Hobbs et al., 1993, Proc. Nat. Acad. Sci. USA, 90, 6909-6913), vinylogous polypeptides (Hagihara et al., 1992, J. Amer. Chem. Soc., 114, 6568), nonpeptidal peptidomimetics with glucose scaffolding (Hirschmann et al., 1992, J. Amer. Chem. Soc., 114, 9217-9218), analogous organic syntheses of small compound libraries (Chen et al., 1994, J. Amer. Chem. Soc., 116:2661 (1994)), oligocarbamates (Cho et al., 1993, Science, 261, 1303 (1993)), and/or peptidyl phosphonates (Campbell et al., 1994, J. Org. Chem., 59:658), nucleic acid libraries (see Ausubel, Berger and Sambrook, all supra); antibody libraries (see, e.g., Vaughn et al., 1996, Nat. Biotech., 14(3):309-314, carbohydrate libraries, e.g., Liang et al., 1996, Science, 274:1520-1522, small organic molecule libraries (see, e.g., benzodiazepines, Baum, 1993, C&EN, January 18, page 33. Devices for the preparation of combinatorial libraries are commercially available (see, e.g., 357 MPS, 390 MPS, Advanced Chem Tech, Louisville Ky., Symphony, Rainin, Woburn, Mass., 433 A Applied Biosystems, Foster City, Calif., 9050 Plus, Millipore, Bedford, Mass.). In addition, numerous combinatorial libraries are themselves commercially available (see, e.g., ComGenex (Princeton, N.J.), Asinex (Moscow, RU), Tripos, Inc. (St. Louis, Mo.), ChemStar, Ltd., (Moscow, RU), 3D Pharmaceuticals (Exton, Pa.), Martek Biosciences (Columbia, Md.), etc.).
  • Methylation modifiers are known and have been the basis for several approved drugs. Major classes of enzymes are DNA methyl transferases (DNMTs), histone deacetylases (HDACs), histone methyl transferases (HMTs), and histone acetylases (HATs). DNMT inhibitors azacitidine (Vidaza®) and decitabine have been approved for myelodysplastic syndromes (for a review see Musolino et al., 2010, Eur. J. Haematol. 84, 463-473; Issa, 2010, Hematol. Oncol. Clin. North Am. 24(2), 317-330; Howell et al., 2009, Cancer Control, 16(3) 200-218; which are hereby incorporated by reference in their entirety). HDAC inhibitor, vorinostat (Zolinza®, SAHA) has been approved by FDA for treating cutaneous T-cell lymphoma (CTCL) for patients with progressive, persistent, or recurrent disease (Marks and Breslow, 2007, Nat. Biotech. 25(1), 84-90). Specific examples of compound libraries include: DNA methyl transferase (DNMT) inhibitor libraries available from Chem Div (San Diego, Calif.); cyclic peptides (Nauman et al., 2008, ChemBioChem 9, 194-197); natural product DNMT libraries (Medina-Franco et al, 2010, Mol. Divers., Springer, published online 10 Aug. 2010); HDAC inhibitors from a cyclic a33-tetrapeptide library (Olsen and Ghadiri, 2009, J. Med. Chem. 52(23), 7836-7846); HDAC inhibitors from chlamydocin (Nishino et al., 2006, Amer. Peptide Symp. 9(7), 393-394).
    • 5.8. Methods of Inhibition Using Nucleic Acids
  • A variety of nucleic acids, such as antisense nucleic acids, siRNAs or ribozymes, may be used to inhibit the function of the markers of this invention. Ribozymes that cleave mRNA at site-specific recognition sequences can be used to destroy target mRNAs, particularly through the use of hammerhead ribozymes. Hammerhead ribozymes cleave mRNAs at locations dictated by flanking regions that form complementary base pairs with the target mRNA. Preferably, the target mRNA has the following sequence of two bases: 5′-UG-3′. The construction and production of hammerhead ribozymes is well known in the art.
  • The following Examples further illustrate the invention and are not intended to limit the scope of the invention.
    • 6. EXAMPLES 6.1. Materials and Methods
  • Patients and Tissues:
  • Retrospective clinic-based series of primary formalin-fixed, paraffin-embedded (FFPE) invasive cutaneous melanomas (n=22) or melanocytic nevi (n=27) were obtained from the Pathology Archives at UNC. Collection of tissues and associated patient information was approved by the Institutional Review Board at UNC. An honest broker searched the Pathology Laboratory Database at UNC-Chapel Hill and retrieved specimens collected after Jan. 1, 2001; all specimens were de-identified. All common histologic subtypes of primary cutaneous melanomas were included. Nevi were melanocytic and cutaneous, came from patients without melanoma, and included benign common melanocytic nevi, including intradermal, compound, congenital pattern and dysplastic nevi.
  • Medical Record Information:
  • The UNC melanoma database manager extracted demographic and clinical information from the medical chart, including age, sex, anatomic sites of nevi and melanomas, and Breslow depth and Clark level of melanomas.
  • Standardized Pathology Review and Enrichment of Melanoma or Nevi:
  • Five μm-thick tissue sections were cut from each block containing melanoma or nevus and were mounted on uncoated glass slides. A hematoxylin and eosin (H&E) slide of each melanoma or nevus specimen was reviewed by an expert dermatopathologist to confirm diagnosis, classify histologic subtype, and score standard histopathology features (histologic subtype, thickness, ulceration, solar elastosis, etc). In addition, the pathologist reviewed each tissue for histologic parameters that could affect assay performance and quality such as formalin-fixation adequacy, tissue size, percent tumor, and percent necrosis. To selectively isolate melanoma or nevi away from surrounding normal skin, H&E slides were used as guides for manual dissection of melanoma or nevus cells from each tissue section.
  • Cell Lines and Peripheral Blood Leukocytes:
  • The Mel-505 melanoma and MCF-7 breast tumor cell lines were used to establish assay conditions and to assess assay reproducibility and the effects of formalin-fixation and contamination by non-melanocytic cells on methylation profiles. Cell lines were grown in RPMI medium with 10% fetal bovine serum and harvested while in log growth phase. Cells were pelleted and divided into two portions. One portion was used for DNA extraction (non-fixed) and the other pellet was fixed in buffered formalin, embedded in paraffin, and sections were cut from the paraffin blocks and were mounted on uncoated glass slides. Mixtures of DNA obtained from peripheral blood leukocytes (PBL) and the Mel-505 cell line in varying proportions were used to evaluate the effect of contamination of the methylation profile of the Mel-505 melanoma cell line by ‘non-melanocytic’ PBL cells.
  • Normal Skin:
  • FFPE normal skin tissue was obtained from breast reduction specimens under IRB approval.
    • 6.2. DNA Preparation
  • DNA was prepared from formalin-fixed nevi, melanoma, or normal skin tissues, or cell line pellets as previously published (Thomas et al., 2007, Cancer Epidemiol Biomarkers Prev. 16, 991-977). DNA was purified from non-fixed cell lines or peripheral blood leukocytes using the FlexiGene DNA according to the manufacturer's instructions (Qiagen, Valencia, Calif.). 6.3. Bisulfite Treatment of DNA
  • Sodium bisulfite modification of DNA obtained from FFPE or non-fixed cells was performed using the EZ DNA Methylation Gold kit (Zymo Research, Orange, Calif.). Approximately 500-1000 ng DNA from each tissue specimen was mixed with 130 μl of CT Conversion Reagent in a PCR tube and cycled in a thermal cycler at 98° C. for 10 minutes, 64° C. for 2.5 hours, and stored at 4° C. for up to 20 hours. The sample was then mixed with 600 μl M-binding buffer and spun through the Zymo-Spin IC column for 30 seconds (≧10,000×g). The column was washed with 100 μl of M-Wash buffer, spun, and incubated in 200 μl of M-Desulphonation buffer for 15-20 minutes. The column was then spun for 30 seconds (at ≧10,000×g), washed twice with 200 ul M-Wash buffer, and spun at top speed. The sample was eluted from the column with 10 μl M-Elution buffer and stored in a −20° C. freezer prior to use in the Illumina GoldenGate Methylation assay. After bisulfite treatment, DNA quantity and concentration were measured by a Nanodrop spectrophotometer, and DNA concentration adjusted to 50-60 ng/μl.
    • 6.4. Illumina GoldenGate Cancer Panel I Methylation Analysis
  • Array-based DNA methylation profiling was accomplished using the Illumina GoldenGate Cancer Panel I methylation bead array (Illumina, San Diego, Calif.) to simultaneously interrogate 1505 CpG loci associated with 807 cancer-related genes. Bead arrays were run in the Mammalian Genotyping Core laboratory at the University of North Carolina. The Illumina GoldenGate methylation assay was performed as described previously (Bibikova et al., 2006, Genome Res., 16, 383-393). Two allele-specific oligonucleotides (ASO) and 1 locus-specific oligo (LSO) are designed to interrogate each CpG site, with the LSO containing a sequence which corresponds to a specific address on the BeadArray. Bisulfite-converted DNAs were biotinylated and bound to paramagnetic particles, hybridized to ASO and LSO probes, and the hybridized ASO oligos were extended in a methylation-specific fashion, then ligated to the LSO probe to create amplifiable templates. The joining of two fragments to create a PCR template provides an added level of locus specificity. The PCR that followed used 2 fluorescently-labeled (Cy3, Cy5) and biotinylated universal PCR primers corresponding to the ASO sequences (P1, P2) and a common P3 primer that binds to the LSO sequence. Labeled amplicons were bound to paramagnetic particles and denatured, then after filtering out the biotinylated strands, the fluor-labeled strands were hybridized to the Sentrix BeadArray under a temperature gradient, and imaged using the BeadArray Scanner (Illumina). Methylation status of the interrogated CpG sites was determined by comparing the ratio of the fluorescent signal from the methylated allele to the sum from the fluorescent signals of both methylated and unmethylated alleles. Controls for methylation status used on each bead array included the Zymo Universal Methylated DNA Standard as the positive, fully-methylated control, and a GenomePlex (Sigma) whole genome amplified (WGA) DNA used as the negative, unmethylated control.
    • 6.5. Bioinformatics and Statistical Analysis
  • The data were assembled using the GenomeStudio Methylation software from Illumina (San Diego, Calif.). All array data points were represented by fluorescent signals from both methylated (Cy5) and unmethylated (Cy3) alleles. Background intensity computed from the negative control was subtracted from each data point. The methylation level of individual interrogated CpG sites was determined by the β-value, defined as the ratio of fluorescent signal from the methylated allele to the sum of the fluorescent signals of both the methylated and unmethylated alleles and calculated as β=max(Cy5,0)/(|Cy5|+|Cy3|+100). β values ranged from 0 in the case of completely unmethylated to 1 in the case of fully methylated DNA. The BeadStudio Methylation Module software (Illumina) was used to create scatter plots to examine the relationship between cell line replicates and between FFPE and non-fixed samples. The correlation coefficient, R2, was calculated for each comparison.
  • For studies of melanomas and nevi, average methylation β values were derived from the multiple β values calculated for each CpG site within the melanoma (n=22) or nevus (n=27) groups. Prior to clustering or further statistical analysis, filtering was performed to remove a total of 478 probes that corresponded to 68 CpG sites on the X chromosome and 410 that were reported to contain a single nucleotide polymorphism or repeat within the recognition sequence thus making the probes unreliable in at least some samples (Byun et al., 2009, Hum. Mol. Genet. 18, 4808-4817). In addition, a detection p-value computed by GenomeStudio and representing the probability that the signal from a given CpG locus is distinguishable from the negative controls was used as a metric for quality control for sample performance. β values with a detection p-value greater than 10−5 were considered unreliable and set to be missing (Marsit et al, 2009, Carcinogenesis, 30, 416-422). Two nevus samples with more than 25% missing β values and 39 CpG loci with more than 20% missing samples were excluded from analysis. The final data contained 988 CpG loci in 646 genes and 49 samples (22 melanomas and 27 moles).
  • All subsequent statistical analyses were carried out using the R package (http://www.r-project.org/). For exploratory/visualization purposes, unsupervised hierarchical clustering using the Euclidean metric and complete linkage was performed. To adjust for age or gender effect, a linear model was fitted to the logit transformed β-values using age and gender as covariates in comparing the methylation levels between melanomas and moles at each locus. Bonferroni correction was used to adjust for multiple comparisons, i.e., significant loci were selected with p-value 0.05/988=5.06×10−5, with an additional filter of mean adjusted β-value difference 0.2 between melanomas and moles to be clinically significant. In addition, the area under the receiver operating characteristics curve (AUC) was computed to summarize the accuracy of correctly classifying melanomas and moles using these significant loci. The Prediction Analysis of Microarrays (PAM) approach (Tibshirani et al. 2002, Proc. Nat. Acad. Sci. USA, 99, 6567-6572) was carried out to assess the classification of melanoma and nevus samples by the method of nearest shrunken centroids.
  • Gene Ontology Analysis:
  • The DAVID Bioinformatics Resources 6.7 Functional Annotation Tool (http://david.abcc.ncifcrf.gov/home.jsp) was used to perform gene-GO term enrichment analysis to identify the most relevant GO terms associated with the genes found to be differentially methylated between nevi and malignant melanomas. Gene function was also investigated using GeneCards (http://www.genecards.org/).
    • 6.6. Results
  • Optimization and Validation of Illumina Methylation Array in Cell Lines:
  • We optimized conditions for performance of the Illumina GoldenGate Methylation Cancer Panel I array, which is designed to detect methylation at 1505 CpG sites in the promoters and regulatory regions of 807 cancer related genes. We also evaluated array reproducibility, and the impact of formalin fixation and intermixture of melanocytic with non-melanocytic DNA on methylation profiles. In testing a range of bisulfite-treated DNA quantities from 25 to 500 ng, we determined that a minimum of 200 ng non-fixed DNA or 250 ng of formalin-fixed DNA was needed to successfully perform array profiling, and that sufficient DNA was recoverable from the majority of FFPE melanoma or nevus tissues.
  • We found very high reproducibility between non-fixed cell lines and the same lines which had undergone the FFPE process. Cell lines were pelleted, formalin-fixed, and paraffin-embedded just as tissue is in the clinical setting to create FFPE-processed equivalents for cell lines. Shown in FIGS. 1A-1C are replicate methylation array profiles of non-formalin-fixed MCF-7 breast tumor cell DNA, formalin-fixed DNA from the Mel-505 melanoma cell line, as well as methylation profiles from non-fixed versus FFPE Mel-505 DNA. Each of these array replicates produced was highly reproducible, showing r2 values of ≧0.98. We optimized the Illumina GoldenGate Methylation assay using 250-500 ng, and tested assay performance on matched pairs of frozen and/or FFPE cell line DNA. Using ≧250 ng DNA, methylation profiles were compared and showed very high correlation between frozen duplicates of 8 cell line DNAs (r2=0.98), 20 matched FFPE and frozen cell line DNAs (r2=0.98), and 14 FFPE duplicate DNA samples (r2=0.97). The FFPE tissues produced methylation profiles very similar to those from matched frozen specimens, and that 250 ng or more of FFPE DNA provides suitable template for methylation profiling.
  • We conducted experiments to gauge the proportion of melanoma cell line Mel-505 DNA that must be present in a tumor/normal DNA mixture in order for the melanoma methylation profile to be evident. In FIGS. 1D-1I, the Mel-505 cell line DNA was diluted with increasing proportions (from 0 to 50%) of DNA from normal peripheral blood leukocytes (PBLs) (90% Mel-505/10% PBL, 80% Mel-505/20% PBL, 70% Mel-505/30% PBL, 60% Mel-505/40% PBL, 50% Mel-505/50% PBL), and each mixture was plotted against the profile for pure (100%) Mel-505 cell line DNA. The Mel-505 cell line profile was evident even after dilution with up to 30% PBL DNA (70% Mel-505/30% PBL mixture) (r2=0.89), indicating that a moderate level of contamination of melanocytic cells by normal DNA will not significantly disrupt the melanoma methylation pattern. This result provides a guideline for estimating the necessary purity of tumor DNA to achieve methylation array results that are representative of melanocytic target DNA.
  • Characteristics of Patients with Benign Nevi or Malignant Melanoma:
  • Illumina methylation array analysis was performed on 27 FFPE benign nevi, 22 FFPE primary malignant melanomas and 9 FFPE lymph node metastatic melanomas. The patient characteristics as well as histologic and clinical features of these tissues are detailed in Table 1 below. The mean age of nevus patients (29 years) was significantly less than melanoma patients (61 years; p<0.0001). Among patients with nevi, 83% were younger than 40 yrs, whereas only 27% of melanoma patients were younger than 40 yrs. Forty-one percent of nevus patients and 50% of melanoma patients were male. The anatomic site of nevi differed significantly from that of melanomas (p=0.1300), with nevi occurring predominantly on the head and neck (HN)(35%) or trunk (52%), and melanomas occurring mostly on either the trunk (36%) or an extremity (41%). Among nevi, 38% were classified histologically as intradermal melanocytic nevi, 31% were described as compound melanocytic nevi, and 21% were identified as compound melanocytic nevi with congenital pattern. Only 7% of nevi were classified as being compound dysplastic nevi with slight atypia. Among melanomas, 50% were of the superficial spreading histologic type, 14% were lentigo maligna, 14% were acral lentiginous, 9% were nodular, and 9% were spindle cell melanoma. The melanomas consisted mostly of deeper lesions, with 32% having a Breslow depth of ≦1.5 mm, and 68% having Breslow depth of >1.5
  • TABLE 1
    Clinical and histologic characteristics of 27 non-malignant nevi and 22 primary
    cutaneous malignant melanomas and 9 lymph node metastatic melanomas evaluated
    for DNA promoter methylation
    Breslow
    Histologic Age depth Presence of
    No Lesion Type/Features yrs Sex Site (mm) Lymphocytes
    001 Melanoma SSM 89 Male extremity 4.6 absent
    002 Melanoma SSM 33 Male trunk 0.82 1-2
    003 Melanoma SSM 81 female HN 3.65 absent
    004 Melanoma SSM 38 female trunk 5.7 absent
    005 Melanoma SC 76 Male extremity 1.3 1-2
    006 Melanoma NM 26 Male trunk 1.0 3
    007 Melanoma SSM 43 Male trunk 0.59 3
    009 Melanoma SSM 35 Male trunk 1.3 3
    010 melanoma SSM 78 Male extremity 4.55 absent
    011 melanoma SSM 71 female extremity 3.5 absent
    013 melanoma LMM 82 female HN 1.78 1-2
    014 melanoma LMM 83 female HN 3.65 absent
    016 melanoma SSM 70 Male extremity 0.93 1-2
    017 melanoma SSM 76 Male trunk 1.25 1-2
    019 melanoma NM 68 female trunk 2.6 absent
    021 melanoma SC 47 female HN 10.0 absent
    022 melanoma ALM 84 female extremity 7.1 absent to
    minimal
    117 melanoma ALM 31 female extremity 5.4 absent to
    minimal
    124 melanoma LMM 67 female HN 5.0 1-2
    126 melanoma ALM 69 Male trunk 5.25 absent
    503 melanoma SSM 36 female extremity 4.6 1-2
    504 melanoma UNCL 49 Male extremity 4.35 absent
    475 nevus compound dysplastic 18 Male HN na absent
    nevus w/ slight atypia
    476 nevus compound nevus 38 Female HN na absent
    477 nevus compound nevus 48 Female extremity na absent
    478 nevus compound nevus 22 Female extremity na absent
    479 nevus compound nevus 34 Male HN na absent
    480 nevus compound nevus 27 Male HN na absent
    481 nevus compound nevus 21 Female extremity na absent
    482 nevus compound nevus 25 Male trunk na absent
    483 nevus compound nevus 13 Male trunk na absent
    484 nevus intradermal nevus 32 Female HN na absent
    485 nevus intradermal nevus 21 Female HN na absent
    486 nevus intradermal nevus 41 Female HN na absent
    487 nevus intradermal nevus 26 Female trunk na absent
    488 nevus intradermal nevus 89 Female trunk na absent
    489 nevus intradermal nevus 13 Female HN na absent
    490 nevus intradermal nevus 26 Female extremity na absent
    492 nevus intradermal nevus 20 Female trunk na absent
    493 nevus intradermal nevus 15 Female trunk na absent
    494 nevus compound nevus 33 Female trunk na absent
    495 nevus compound nevus w/ 9 Male HN na absent
    congenital pattern
    496 nevus compound nevus 43 Male trunk na absent
    497 nevus compound nevus w/ 23 Male trunk na absent
    congenital pattern
    498 nevus compound nevus w/ 18 Female trunk na absent
    congenital pattern
    499 nevus compound nevus w/ 66 Male HN na absent
    congenital pattern
    500 nevus compound cutaneous 22 Female trunk na absent
    501 nevus compound nevus w/ 13 Female trunk na absent
    congenital pattern
    502 nevus compound nevus w/ 11 Male trunk na absent
    congenital pattern
    029 melanoma metastasis 83 Male cervical na
    030 melanoma metastasis 82 male cervical na
    049 melanoma metastasis 73 male axillary na
    061 melanoma metastasis 80 female lymph na
    node
    107 melanoma metastasis 47 male cervical na
    114 melanoma metastasis 62 female axillary na
    116 melanoma metastasis 91 female inguinal na
    119 melanoma metastasis 31 male inguinal na
    122 melanoma metastasis 22 female axillary na
    • 6.7. Comparison of Methylation Profiles in Benign Nevi and Malignant Melanomas
  • We performed Illumina GoldenGate Cancer Panel I methylation profiling to evaluate promoter methylation patterns in 27 benign nevi and 22 primary melanomas. Illumina methylation array results were subjected to filtering to remove 68 probes that corresponded to CpG sites on the X chromosome and 410 probes that were reported to contain a SNP or repeat (Byun et al, 2009), thus making them unreliable in some samples. Additionally, β values with a detection p-value greater than 10−5 were considered unreliable and set as missing data points (Marsit et al, 2009); using this criterium, two nevus samples with more than 25% missing 13 values as well as 39 CpG loci with β values missing in more than 20% missing samples were excluded from analysis. The final data set consisted of 988 CpG loci within 646 genes in 49 specimens (22 melanomas and 27 moles).
  • Unsupervised hierarchical clustering was used to compare methylation patterns at 988 CpG loci in benign nevi and malignant melanomas. Clustering produced a clear separation of melanomas from benign nevi, with two major clusters of nevi and at least four clusters of melanomas identified, suggesting that the methylation signature of melanomas is fundamentally distinct from that of nevi. Using class comparison analyses, 75 CpG sites in 63 genes were identified that differed significantly (with P values of ≦0.05) between nevi and melanomas after Bonferroni correction for multiple comparisons; a list of these 75 loci is provided in Table 2. After further adjustment for patient age and sex, we identified a total of 29 CpG loci in 23 genes that differed significantly between melanomas and nevi; these included 22 CpG loci that were significantly hypomethylated and 7 CpG loci that were significantly hypermethylated in melanoma. The heatmap based on supervised clustering of the 29 differentially methylated CpG loci in nevi and melanomas is shown in FIG. 2. The loci that significantly distinguished melanomas from nevi based on methylation were KCNK4, GSTM2, TRIP6 (2 sites), FRZB, COL1A2, NPR2, which showed hypermethylation, and CARD15/NOD2, KLK10, MPO, EVI2A, EMR3 (2 sites), HLA-DPA1, PTHR1, IL2, TNFSF8, LAT, PSCA, IFNG, PTHLH, three sites in RUNX3 (3 sites), ITK, CD2, OSM (2 sites), and CCL3, which showed hypomethylation in melanomas compared with nevi.
  • TABLE 2
    75 CpG sites from the Illumina GoldenGate Methylation Cancer Panel
    I array that show significant differences in methylation between
    melanomas and benign nevi after Bonferroni correction for
    multiple comparisons
    TargetID Raw_p Bonferroni_p FDR_p
    RUNX3_P393_R 4.02E−14 3.98E−11 1.48E−11
    CD2_P68_F 8.05E−14 7.95E−11 1.48E−11
    MPO_P883_R 8.05E−14 7.95E−11 1.48E−11
    RUNX3_E27_R 8.05E−14 7.95E−11 1.48E−11
    RUNX3_P247_F 8.96E−14 8.86E−11 1.48E−11
    OSM_P188_F 1.61E−13 1.59E−10 1.99E−11
    TNFSF8_E258_R 2.82E−13 2.78E−10 3.09E−11
    PTHLH_E251_F 4.83E−13 4.77E−10 4.77E−11
    ITK_E166_R 2.70E−12 2.66E−09 2.22E−10
    PECAM1_P135_F 3.68E−11 3.64E−08 2.27E−09
    CCL3_E53_R 4.88E−11 4.82E−08 2.68E−09
    EVI2A_E420_F 4.88E−11 4.82E−08 2.68E−09
    ITK_P114_F 1.09E−10 1.08E−07 4.90E−09
    LAT_E46_F 1.41E−10 1.39E−07 5.81E−09
    EVI2A_P94_R 9.23E−10 9.12E−07 3.04E−08
    IL2_P607_R 2.05E−09 2.03E−06 6.34E−08
    TDG_E129_F 3.23E−09 3.19E−06 9.37E−08
    IFNG_P459_R 6.90E−09 6.82E−06 1.57E−07
    GABRA5_P1016_F 1.22E−08 0.000012048 2.68E−07
    EMR3_P39_R 1.75E−08 1.72E−05 3.52E−07
    EMR3_E61_F 2.08E−08 2.06E−05 4.11E−07
    DSG1_P159_R 2.94E−08 2.90E−05 5.59E−07
    HLA-DPA1_P28_R 3.48E−08 3.44E−05 6.38E−07
    OSM_P34_F 4.58E−08 0.000045277 8.23E−07
    ALOX12_E85_R 4.87E−08 4.81E−05 8.29E−07
    DES_E228_R 4.87E−08 4.81E−05 8.29E−07
    PTK7_E317_F 1.09E−07 0.000107353 1.60E−06
    KCNK4_E3_F 1.27E−07 0.000125429 1.72E−06
    MMP10_E136_R 1.27E−07 0.000125429 1.72E−06
    KLK10_P268_R 1.48E−07 0.000146312 1.95E−06
    SNURF_P2_R 1.48E−07 0.000146312 1.95E−06
    COL1A2_E299_F 2.01E−07 0.000198158 2.48E−06
    MMP2_P303_R 2.70E−07 0.00026676 3.21E−06
    FRZB_P406_F 3.10E−07 0.000306716 3.59E−06
    CASP8_E474_F 4.17E−07 0.000412183 4.74E−06
    GSTM2_P453_R 4.40E−07 0.000434777 4.94E−06
    THBS2_P605_R 4.85E−07 0.000479408 5.33E−06
    EPHA2_P203_F 5.54E−07 0.000547104 5.82E−06
    GNMT_P197_F 5.54E−07 0.000547104 5.82E−06
    PTHR1_P258_F 5.54E−07 0.000547104 5.82E−06
    PSCA_E359_F 1.26E−06 0.001240291 1.22E−05
    CARD15_P302_R 1.63E−06 0.001613456 1.5079E−05 
    DSG1_E292_F 2.06E−06 0.002037049 1.85E−05
    IPF1_P750_F 2.11E−06 0.002089181 1.85E−05
    MUSK_P308_F 2.11E−06 0.002089181 1.85E−05
    SNURF_E256_R 2.11E−06 0.002089181 1.85E−05
    ARHGDIB_P148_R 2.40E−06 0.002373277 2.05E−05
    COL1A1_P117_R 2.40E−06 0.002373277 2.05E−05
    TRIP6_P1274_R 2.40E−06 0.002373277 2.05E−05
    MEST_P62_R 3.50E−06 0.003456272 2.86E−05
    SHB_P691_R 3.96E−06 0.003909276 3.18E−05
    SYK_P584_F 3.96E−06 0.003909276 3.18E−05
    SNURF_P78_F 5.05E−06 0.004985595 3.96E−05
    CDH13_P88_F 5.79E−06 0.005720768 4.47E−05
    TNFSF8_P184_F 7.21E−06 0.007126004 5.48E−05
    BMPR1A_E88_F 8.11E−06 0.008011205 6.07E−05
    OPCML_P71_F 8.37E−06 0.008269514 6.22E−05
    HBII-52_P563_F 9.11E−06 0.008997683 6.57E−05
    PWCR1_P357_F 9.11E−06 0.008997683 6.57E−05
    TRIP6_P1090_F 9.11E−06 0.008997683 6.57E−05
    CD86_P3_F 1.02E−05 0.010095984 7.2633E−05 
    HOXA11_P698_F 1.02E−05 0.010095984 7.2633E−05 
    NEFL_E23_R 1.15E−05 0.011317697 8.08E−05
    PTK6_E50_F 1.28E−05 0.012675435 8.56E−05
    ZIM2_P22_F 1.28E−05 0.012675435 8.56E−05
    SEMA3B_E96_F 1.44E−05 0.014183028 9.52E−05
    ALOX12_P223_R 1.60E−05 0.01585551 0.000105
    NPR2_P1093_F 1.60E−05 0.01585551 0.000105
    LOX_P313_R 1.64E−05 0.016180651 0.00010645
    MST1R_P87_R 2.00E−05 0.019762343 0.0001275
    SERPINA5_E69_F 2.00E−05 0.019762343 0.0001275
    TNFRSF10D_E27_F 3.08E−05 0.030382223 0.00018989
    PGR_E183_R 4.21E−05 0.041578421 0.00024897
    RARA_E128_R 4.21E−05 0.041578421 0.00024897
    HPN_P374_R 4.40E−05 0.043487012 0.00025885
    29 bolded loci were still significant after adjustment for age and sex.
    • 6.8. PAM Analysis to Identify CpG Loci Predictive of Melanoma
  • From among the 29 CpG sites that significantly distinguished melanomas from benign nevi, we selected a panel of markers for systematic testing in prediction models. Prediction Analysis for Microarray (PAM) was carried out to assess the classification of melanoma and nevus samples by the method of nearest shrunken centroids. The PAM algorithm automatically identifies CpG loci that contribute most to the melanoma classification. Using 10-fold cross-validation to train the classifier, the optimal shrinkage threshold was chosen to be 4.28 with 12 CpG loci required for optimal classification. This approach yielded a zero cross-validation error, with no misclassification. The 12 CpG loci identified by PAM analysis that provided the most accurate prediction of melanoma were: RUNX3_P393_R, RUNX3_P247_F, RUNX3_E27_R, COL1A2_E299_F, MPO_P883_R, TNFSF8_E258_R, CD2_P68_F, EVI2A_P94_R, OSM_P168_F, ITK_P114_F, FRZB_P406_F, ITK_E166_R. All but one locus (ITK_E166_R) exhibited mean β differences between melanomas and nevi of ≧0.2.
  • The box plots shown in FIGS. 3A-3L display the mean, range, and standard deviation of β values in nevi and melanomas for the 12 CpG sites that are highly predictive of melanoma as determined by PAM analysis. For most CpG loci showing hypomethylation in melanomas compared with benign nevi, mean methylation β values were very high (nearly 1.0), indicating that these CpG sites were uniformly highly methylated in nevi, however, methylation was lost to varying degrees in primary melanomas. Among the CpG loci exhibiting hypermethylation in melanomas, FRZB_P406_F and COL1A2_E299_F, were poorly methylated in nevi, having mean β values near 0.1, but showed considerably higher methylation in many melanomas, with mean β values between 0.6 and 0.7.
  • Sensitivity analysis conducted using Receiver Operator Characteristic (ROC) curves are shown in FIGS. 4A-4O which plot the sensitivity versus the specificity of the 12 CpG loci identified by PAM analysis. The area under the curve (AUC) ranged from 0.89 to 0.90 for the 2 hypermethylated loci, and from 0.96 to 1.00 for the 10 hypomethylated loci. In particular, two of the RUNX3 probes (RUNX3_P247_F and RUNX3_P393_R) exhibited both 100% sensitivity and 100% specificity in identifying melanomas. The sensitivity, specificity and AUC for all 29 CpG loci that differed significantly after adjustment between melanomas and nevi, including the 12 predictive loci identified by PAM analysis, are shown in Table 3A. Data on sequences showing differences in methylation levels (β values) may be found in Table 6 for a combined analysis where metastases were included with melanomas. Descriptions of sequences, methylation sites from the Illumina array and gene names may be found in Table 4A and 4B for the melanoma vs. benign nevi comparison. Data for the metastases vs. benign nevi comparison may be found in Table 5A and 5B (Section 6.10). Some additional specific sequences methylated in the metastatic samples may be found in Tables 7A and 7B. Specific sequences and methylation sites for other CpG probes may be obtained from the gene list for the Illumina GoldenGate Cancer Panel 1.
  • To assess the possibility that methylation differences between melanomas and nevi could result in part from contamination by non-melanocytic DNA, e.g., lymphocytic infiltration of the melanoma specimens or contamination of small melanocytic specimens by normal surrounding skin, the study pathologist estimated the degree of lymphocytic infiltration in melanocytic specimens (Table 1). In addition, we compared the mean methylation β profiles in 4 peripheral blood leukocyte (PBL) samples and 2 normal skin specimens with those of nevi and melanomas (data not shown). Significant lymphocytic presence was noted in only 2 melanomas and none of the nevi, making it unlikely that differential methylation involving immune loci was related to the infiltration by tumor-associated lymphocytes. Methylation profiles of PBL samples showed comparable levels of methylation among the 4 specimens at individual CpG loci.
    • 6.9. Functions of Genes Differentially Methylated in Melanomas and Nevi
  • We explored the major functions of the 23 genes (with 29 CpG sites) that most significantly distinguished melanomas from benign nevi. Table 3B provides gene functional information obtained through gene ontology searches using the DAVID Bioinformatics Resources 6.7 (http://david.abcc.ncifcrf.gov/home.jsp) and the human gene database, GeneCards (http://www.genecards.org). Details on the mean β in nevi and melanomas, mean β differences, adjusted p-values, and AUC (and the sensitivity and specificity of melanoma prediction) for each gene are presented in Table 3A. While the number of genes identified was too small to fully evaluate functional pathways, it was of interest that half (β of 23) possessed immune response or inflammation pathway functions, including roles in T-cell signaling and/or natural killer cell cytotoxicity (IFNG, IL2, ITK, LAT, CD2, CCL3, TNFSF8, HLA-DPA1), myeloid-myeloid cell interactions (EMR3), neutrophil microbicidal activity (MPO), innate immunity (CARD15/NOD2), and NF-κB activation (TRIP6, OSM, CARD15/NOD2). Three genes are involved in thyroid (TRIP6) or parathyroid (PTHLH, PTHR1) hormonal regulation. Several other genes have well-characterized roles in cancer cell growth, cell adhesion, or apoptosis (RUNX3, FRZB, TNFSF8, KLK10, PSCA, OSM, COL1A2). The 3 CpG sites located within the RUNX3 gene all exhibited significantly lower methylation in melanomas compared with nevi even though RUNX3 has been considered a tumor suppressor gene and might be expected to display promoter hypermethylation, rather than hypomethylation, in malignancy (Kitago et al., 2009, Clin. Cancer Res. 15, 2988-2994). However, more recent studies suggest that RUNX3 may have both tumor suppressor and oncogenic functions depending on the cellular context (Chuang and Ito, 2010, Oncogene 29, 2605-2615).
  • TABLE 3A
    Twenty-nine CpG loci exhibiting significant promoter methylation
    differences between melanomas and benign nevi
    Nevus Melanoma
    Gene CpG/ mean mean Mean β
    Symbol Probe β β P value Difference AUC Skin PBL
    Hypermethylated in melanomas compared with nevi (n = 7)
    COL1A2 E299_F 0.0386 0.5093 4.1 ×10−5 +0.4707 0.9007 U U
    FRZB P406_F 0.0255 0.2831 1.4 ×10−2 +0.2576 0.8986 U U
    GSTM2 P453_R 0.1548 0.6087 6.3 ×10−3 +0.4539 0.9186 P M
    KCNK4 E3_F 0.0646 0.4014 2.6 ×10−3 +0.3369 0.9057 U M
    NPR2 P1093_F 0.5459 0.8224 1.8 ×10−2 +0.2765 0.8434 P M
    TRIP6 P1090_F 0.0619 0.5741 6.3 ×10−5 +0.5121 0.8518 U M
    TRIP6 P1274_R 0.1584 0.6660 2.7 ×10−3 +0.5076 0.8704 U M
    Hvpomethylated in melanomas compared with nevi (n = 22)
    CCL3 E53 _R 0.9227 0.7180 5.7 ×10−5 −0.2047 0.9714 P M
    CARD15 P302 R 0.5146 0.0962 3.1 ×10−2 −0.4184 0.8754
    EV12A P94_R 0.7358 0.2121 1.3 ×10−3 −0.5237 0.9592 M U
    HLA- P28 _R 0.8886 0.5277 3.3 ×10−2 −0.3609 0.9191 U
    IFNG P459_R 0.9150 0.6334 7.9 ×10−9 −0.2915 0.9630 M M
    ITK P114_F 0.9289 0.6480 2.7 ×10−6 −0.2809 0.9663 M M
    ITK E166 _R
    LAT E46 _F 0.8780 0.4948 1.8 ×10−2 −0.3832 0.9646 P U
    IL2 P607 _R 0.8922 0.6022 9.0 ×10−3 −0.2900 0.9489 M
    CD2 P68 _F 0.9620 0.7382 1.3 ×10−7 −0.2238 0.9983 M U
    MPO P883_R 0.7713 0.1750 2.4 ×10−6 −0.5963 0.9983 P/U U
    EMR3 E61_F 0.9019 0.4205 1.3 ×10−3 −0.4814 0.9242 M P
    EMR3 P39_R 0.9210 0.6379 2.0 ×10−3 −0.2831 0.9259 M P
    OSM P188 _F 0.9560 0.7516 3.6 ×10−6 −0.2044 0.9966
    OSM P34 _F 0.9000 0.6988 3.0 ×10−2 −0.2008 0.9206 U U
    TNFSF8 E258_R 0.9552 0.6155 1.6 ×10−7 −0.3517 0.9949 M U
    PTHLH E251_R 0.9074 0.5488 5.8 ×10−6 −0.3586 0.9933
    PTH R1 P258_F 0.8128 0.5253 4.5 ×10−3 −0.2875 0.8889 M
    RUNX3 P393 _R 0.9595 0.6912 3.3 ×10−8 −0.2684 1.0000 M M
    RUNX3 E27 _R 0.9550 0.6341 6.5 ×10−8 −0.3209 0.9983 M M
    RUNX3 P247_F 0.9599 0.6005 1.1 ×10−8 −0.3594 1.0000 M M
    PSCA E359_F 0.8366 0.6169 5.2 ×10−3 −0.4105 0.8788 U
    KLK10 P268_R 0.6305 0.2200 4.4 ×10−2 −0.3397 0.9040 U
    The 29 CpG loci/genes shown were found to exhibit significantly different methylation between melanomas and nevi after adjustment for age, sex, and Bonferroni correction for multiple comparisons. These loci, with the exception of TK_E166_R, also had mean methylation β value differences between nevi and melanomas of ≧0.2. All loci except ITK_E166_R exhibited. Probes were ranked by significance (adjusted P value) within each of the hypermethylated and hypomethylated groups. P value, nevus mean β, and melanoma mean β were each adjusted for age, sex, multiple comparisons using Bonferroni correction. AUC; area under the ROC curve. Methylation status in normal skin and peripheral blood leukocytes (U; unmethylated (~0.0-0.3), PM; partially methylated (~0.3-0.7), M; highly methylated (~0.8-1.0)).
  • TABLE 3B
    The function/pathway description for the twenty-nine CpG loci
    Gene
    Symbol Function/Pathway Description
    Hypermethylated in melanomas compared with nevi (n = 7)
    COL1A2 extracellular matrix, cell commun, focal adhesion
    FRZB −regulator of Wnt signaling; cell growth & differentiation
    GSTM2 carcinogen & oxidative metabolism
    KCNK4 potassium ion transport
    NPR2 receptor for several small natriuretic peptides
    TRIP6 +reg cell migration, release of cytopasmic NF-kB
    TRIP6 +reg cell migration, release of cytopasmic NF-kB
    CCL3 chemokine activity, immune response, upreg in tumors
    CARD15 Immune response to LPS, resulting in NF-kB activation
    EV12A Viral insertion site Evi12 mapped to NF1 gene region and
    noncoding region of GNN
    HLA-DPA1 cell adhesion, antigen presentation, immune response
    IFNG NK cell-mediated cytotox, T cell receptor signaling
    ITK T cell receptor proliferation & differentiation
    ITK T cell receptor proliferation & differentiation
    LAT NK cell-mediated cytotox, T cell receptor signaling
    IL2 Cytokine that regulates T-cell proliferation
    CD2 Mediates adhesion to T cells
    MPO Neutrophil oxidative metabolism, anti-apoptotic
    EMR3 granulocyte marker, involved in myeloid - myeloid
    interactions during immune responses
    EMR3 granulocyte marker, involved in myeloid - myeloid
    interactions during immune responses
    OSM reg cell growth & cytokine production, Jak/STAT pathway
    OSM reg cell growth & cytokine production, Jak/STAT pathway
    TNFSF8 cytokine, induces T-cell proliferation, pro-apoptosis
    PTHLH parathyroid hormone signaling
    PTHR1 parathyroid hormone signaling
    RUNX3 −regulator of cell proliferation, pro-apoptosis
    RUNX3 −regulator of cell proliferation, pro-apoptosis
    RUNX3 −regulator of cell proliferation, pro-apoptosis
    PSCA membrane antigen, apoptosis, up- or downregulated in
    cancer
    KLK10 secreted serine protease, tumor suppressor
  • TABLE 4A
    Table 4A shows the accession numbers; specific single CpG coordinate;
    presence or absence of CpG islands; specific sequences used in the
    Illumina GoldenGate array experiments; and the synonyms for the genes
    hypomethylated in melanoma. All Accession numbers and location are
    based on Ref. Seq. version 36.1.
    Probe_ID Gid Accession Gene_ID Chrm CpG_Coor Dist_to_TSS CpG_isl
    ARHGDIB_P148_R 56676392 NM_001175.4 397 12 15005977 −148 N
    BMPR1A_E88_F 41349436 NM_004329.2 657 10 88506464 88 Y
    CARD15_P302_R 11545911 NM_022162.1 64127 16 49288249 −302 N
    CASP8_E474_F 73623018 NM_001228.3 841 2 201806900 474 N
    CCL3_E53_R 4506842 NM_002983.1 6348 17 31441547 53 N
    CD2_P68_F 31542293 NM_001767.2 914 1 117098557 −68 N
    CD86_P3_F 29029570 NM_006889.2 942 3 123256908 −3 N
    COL1A1_P117_R 14719826 NM_000088.2 1277 17 45634109 −117 Y
    DSG1_E292_F 4503400 NM_001942.1 1828 18 27152342 292 N
    DSG1_P159_R 4503400 NM_001942.1 1828 18 27151891 −159 N
    EMR3_E61_F 23397638 NM_152939.1 84658 19 14646749 61 N
    EMR3_P39_R 23397638 NM_152939.1 84658 19 14646849 −39 N
    EVI2A_E420_F 51511748 NM_001003927.1 2123 17 26672423 420 N
    EVI2A_P94_R 51511748 NM_001003927.1 2123 17 26672937 −94 N
    GABRA5_P1016_F 6031207 NM_000810.2 2558 15 24741680 −1016 N
    HBII-52_P563_F 29171307 NR_001291.1 338433 15 22966406 −563 Y
    HLA-DPA1_P28_R 24797073 NM_033554.2 3113 6 33149384 −28 N
    IFNG_P459_R 56786137 NM_000619.2 3458 12 66840247 −459 N
    IL2_P607_R 28178860 NM_000586.2 3558 4 123597937 −607 N
    ITK_E166_R 21614549 NM_005546.3 3702 5 156540651 166 N
    ITK_P114_F 21614549 NM_005546.3 3702 5 156540371 −114 N
    KLK10_P268_R 22208981 NM_002776.3 5655 19 56215362 −268 N
    LAT_E46_F 62739153 NM_014387.3 27040 16 28903694 46 N
    MMP10_E136_R 4505204 NM_002425.1 4319 11 102156418 136 N
    MMP2_P303_R 75905807 NM_004530.2 4313 16 54070286 −303 Y
    MPO_P883_R 4557758 NM_000250.1 4353 17 53714178 −883 N
    MUSK_P308_F 5031926 NM_005592.1 4593 9 112470652 −308 N
    OPCML_P71_F 59939898 NM_002545.3 4978 11 132907684 −71 N
    OSM_P188_F 28178862 NM_020530.3 5008 22 28993028 −188 Y
    OSM_P34_F 28178862 NM_020530.3 5008 22 28992874 −34 N
    PECAM1_P135_F 21314616 NM_000442.2 5175 17 59817858 −135 Y
    PGR_E183_R 31981491 NM_000926.2 5241 11 100506282 183 N
    PSCA_E359_F 29893565 NM_005672.2 8000 8 143759274 359 N
    PTHLH_E251_F 39995088 NM_198964.1 5744 12 28015932 251 N
    PTHR1_P258_F 39995096 NM_000316.2 5745 3 46893982 −258 N
    PTK6_E50_F 27886594 NM_005975.2 5753 20 61639101 50 Y
    PTK7_E317_F 27886610 NM_002821.3 5754 6 43152324 317 Y
    PWCR1_P357_F 29171309 NR_001290.1 63968 15 22847360 −357 N
    RUNX3_E27_R 72534651 NM_001031680.1 864 1 25164035 27 N
    RUNX3_P247_F 72534651 NM_001031680.1 864 1 25164309 −247 Y
    RUNX3_P393_R 72534651 NM_001031680.1 864 1 25164455 −393 Y
    SEMA3B_E96_F 54607087 NM_004636.2 7869 3 50280140 96 N
    SERPINA5_E69_F 34147643 NM_000624.3 5104 14 94117633 69 N
    SHB_P691_R 4506934 NM_003028.1 6461 9 38059901 −691 Y
    SNURF_E256_R 29540557 NM_005678.3 8926 15 22751484 256 Y
    SNURF_P2_R 29540557 NM_005678.3 8926 15 22751226 −2 Y
    SNURF_P78_F 29540557 NM_005678.3 8926 15 22751150 −78 Y
    SYK_P584_F 34147655 NM_003177.3 6850 9 92603307 −584 N
    TDG_E129_F 56549140 NM_001008411.1 6996 12 102883876 129 Y
    THBS2_P605_R 40317627 NM_003247.2 7058 6 169396667 −605 N
    TNFSF8_E258_R 24119162 NM_001244.2 944 9 116732333 258 N
    TNFSF8_P184_F 24119162 NM_001244.2 944 9 116732775 −184 Y
    ZIM2_P22_F 33354272 NM_015363.3 23619 19 62043909 −22 Y
    SEQ
    Probe_ID ID Input_Sequence
    ARHGDIB_P148_R 1 GCACATGTGCGAGCATGACAGCCCGTGTGA[CG]TGGAGATGCATGAATGTACACGCAAGA
    BMPR1A_E88_F 2 AGGAGGGAGGAGGGCCAAGGG[CG]GGCAGGAAGGCTTAGGCTCG
    CARD15_P302_R 3 AGAGCTCCGAGTCACGTGGCTTGGG[CG]GGCCTCCCCTTCCTGGTGTCCA
    CASP8_E474_F 4 CCTTGCCCAGAGGCTGCGGGCTG[CG]GGTCAAGACATCAGTAGAAGGAGG
    CCL3_E53_R 5 AGCAGGTGACGGAATGTGGGCT[CG]AGTGTCAGCAGAGCCAAGAAAGGACTG
    CD2_P68_F 6 TGTAAAGAGAGGCACGTGGTTAAGCTCT[CG]GGGTGTGGACTCCACCAGTC
    CD86_P3_F 7 AAGTTAGCTGGGTAGGTATACAGTCATTGC[CG]AGGAAGGCTTGCACAGGGTG
    COL1A1_P117_R 8 CGTGCCCCAGCCAATCAGAGCTGCCTGGCC[CG]GCCCCCAATTTGGGAGTTGG
    DSG1_E292_F 9 GAGTGGATTCTGGTAAAAGTCCTTCATAAT[CG]TGCCCATTGTAAACAAGTGAAAACTTT
    DSG1_P159_R 10 CCCATCACCTGTATAACCCT[CG]GTATTTCTGTTCACTTTAAGAGCCTGCCAC
    EMR3_E61_F 11 AGCAAACTGCTTCCCCTCTTT[CG]CCATCAGACTCATGGTTCTGCTTTTCGTTT
    EMR3_P39_R 12 GGGATGATTGAGTTGGTAAACCCTAA[CG]AGGAAATGCCCTGAAAGTTACATCAC
    EVI2A_E420_F 13 AGGAAACCAAACTTAGATCCTT[CG]TAATCCTAATTTAAAACTCCATGGCGATGG
    EVI2A_P94_R 14 CATGACAGGAGGCTTTGTAGAACCAATCCC[CG]CCTCCAGAGCAGGGAGGGTTTT
    GABRA5_P1016_F 15 TGGTAGAGAAATGAAAGCACCACAGTGTGG[CG]GCTCTGGGAGTGCACTGGC
    HBII-52_P563_F 16 GCCCAGGGGCAGGCTATGTGACTGCC[CG]GTCTGCAGCTGTAAGTGGTTTCT
    HLA-DPA1_P28_R 17 GGAACAGTGATGAGGAACTGAGGC[CG]AGTGGAGGCAGATGAGACTGA
    IFNG_P459_R 18 TGCAAATGACCAGAAAGCAAGGAAAGAATG[CG]GTTAAAAGAACAATTTGGTGAGG
    IL2_P607_R 19 CACCTGGGACACTATGAATGTAACAATAAT[CG]TTATGAAATATGATCTTGTTTTTAGTC
    ITK_E166_R 20 TCTCCCTCGAACTTTAAAGTC[CG]CTTCTTTGTGTTAACCAAAGCCAGCCT
    ITK_P114_F 21 GTGAATTTTGAAAGGATGTGGTTT[CG]GCCTTTGACATCAGAGGAGAAGCTC
    KLK10_P268_R 22 AACAGAAACAAGGAAAAAGGGAAACCCA[CG]CCCACTCTGTGGCCGTGAGTGA
    LAT_E46_F 23 GGGTCCTGGATATGGAGGCCA[CG]GCTGCCAGCTGGCAGGTGGC
    MMP10_E136_R 24 GAGCTGGCCAGTAGCTGCAATAGATGCCAC[CG]TTAATTACCTGGGCAAGATCCTTGT
    MMP2_P303_R 25 CCGGCGTCCCTCCTAGTAGTAC[CG]CTGCTCTCTAACCTCAGGACGTCAAGG
    MPO_P883_R 26 GGACAGGAAATCTGGCTGGAGAC[CG]TTGGGCTTCACAGGAAGGAG
    MUSK_P308_F 27 GGAGAGGTGGGGTGCTGAATT[CG]AAGGTCAGGACACCTATACCTCTGGG
    OPCML_P71_F 28 CAGAGCAGTCCTCCAAGGCA[CG]CATTGGCTCCACTCTCCTGAGCGACGG
    OSM_P188_F 29 CGCTCCTCCTCCTGTTTTCTT[CG]AATTCGTTCTTCGAGGTCAGCCCTAC
    OSM_P34_F 30 CAGGCTGGCAGCCACTTTATGCC[CG]CTGGGGCGATTGGCCAACACCTCATGA
    PECAM1_P135_F 31 CAAGGCACAAGTGACATTTGCCTTGG[CG]TTCTTGACCCTCCCTCTGTCTCGC
    PGR_E183_R 32 GAAGTTTGGATGTTGTGTGCCACACTT[CG]ATTTGTCTTAAGGAATGTGTTCC
    PSCA_E359_F 33 TCCTAGGGGGCAGGTAGACAGACTGA[CG]GATGGATGGGCAGAGATGC
    PTHLH_E251_F 34 CCTCAGTTCATTACTGTAAACCC[CG]TACCTTAAAAGACTCGGCTTCTTCTCAC
    PTHR1_P258_F 35 GGCAAGGAGAGGACTATTGAGGCACACACA[CG]TGTCTGGCAGCCTGAGTGGG
    PTK6_E50_F 36 GGCCCAGGTGAGCCTGGTCC[CG]GGACACCATGGCGGGCGGGCGCAGC
    PTK7_E317_F 37 GGGGGCACAGAGCTTGGGAAGCG[CG]GGAGTCCCGTGGGCAAAAG
    PWCR1_P357_F 38 GGAGAAGTTGTCATGGGAGGCCAGC[CG]CCTGCTGGCAAGGAAGATGG
    RUNX3_E27_R 39 CGGCAGCCAGGGTGGAGGAGCTC[CG]AAGCTGACAGAGCAGAGTGGGCC
    RUNX3_P247_F 40 CGGCCTTGGCTCATTGGCTGGGCCG[CG]GTCACCTGGGCCGTGATGTCACGGCC
    RUNX3_P393_R 41 TTTTATTTGTGAGGCTGGCCTCAGCACG[CG]GCCCAAGAAACAGAACTGAAAGCGG
    SEMA3B_E96_F 42 GAGAGATGCTGCTGCGGAAGTCCT[CG]GTGGAGTGTGAGAAGGCAGC
    SERPINA5_E69_F 43 CCCAGGGCTTGAGGGCATGTGAGG[CG]AGGAGAGGATGGACTCTAGAG
    SHB_P691_R 44 GGTGGGAGCCGGGCCCAGCACCAATC[CG]AGAGCAAGGCTAGGGGAGGTC
    SNURF_E256_R 45 AGGCTTGCTGTTGTGCCGTTCTGCCC[CG]ATGGTATCCTGTCCGCTCGCATTGGGGCG
    SNURF_P2_R 46 AGCCTGCCGCTGCTGCAGCGAGTCTGG[CG]CAGAGTGGAGCGGCCGCCGGAGATGCC
    SNURF_P78_F 47 CCTGCACTGCGGCAAACAAGCACGCCTGCG[CG]GCCGCAGAGGCAGGCTGGCG
    SYK_P584_F 48 TTTATTTGGTTGTGGACGTCAGAGC[CG]TCATGGTAAGAAGGAAGCAAAGCCTT
    TDG_E129_F 49 GGGGTTGTCTTACCGCAGTGAGTACCA[CG]CGGTACTACAGAGACCGGCTGCCC
    THBS2_P605_R 50 AACCTGACGTGCAGGCACAGAGCAAGGACT[CG]AGAGAACGAGAAGCAGTGGCAGCAGCT
    TNFSF8_E258_R 51 CCCCAGGTGGCTGGCCACGGAGCC[CG]CCGGCACATGCATGGCTGTGTCTC
    TNFSF8_P184_F 52 CACACACAAAGCAACTTCTGTTT[CG]TTTAGACTCTGCCACAAAACGCCTTC
    ZIM2_P22_F 53 GCAGCTGCCCAGACTTCTGCAC[CG]AGGTGCAGCTCGACGCCTCCTTGTCA
    Probe_ID Synonym cg_no
    ARHGDIB_P148_R D4, GDIA2, GDID4, LYGDI, Ly-GDI, RAP1GN1 cg15450139
    BMPR1A_E88_F ALK3, CD292, ACVRLK3 cg14602437
    CARD15_P302_R CD, ACUG, BLAU, IBD1, NOD2, NOD2B, PSORAS1 cg23486288
    CASP8_E474_F CAP4, MACH, MCH5, FLICE, MGC78473 cg05776114
    CCL3_E53_R MIP1A, SCYA3, G0S19-1, LD78ALPHA, MIP-1-alpha cg21335375
    CD2_P68_F T11, SRBC cg20405187
    CD86_P3_F B70, B7-2, LAB72, CD28LG2, MGC34413 cg01878435
    COL1A1_P117_R OI4, aa 694-711 cg10100754
    DSG1_E292_F DG1, DSG, CDHF4 cg20099449
    DSG1_P159_R DG1, DSG, CDHF4 cg13834042
    EMR3_E61_F . cg15552238
    EMR3_P39_R . cg15746620
    EVI2A_E420_F EVDA, EVI2 cg14414427
    EVI2A_P94_R EVDA, EVI2 cg23352695
    GABRA5_P1016_F . cg02225257
    HBII-52_P563_F RNHBII52 cg21361081
    HLA-DPA1_P28_R HLADP, HLASB, HLA-DP1A cg13031167
    IFNG_P459_R IFG, IFI cg03628117
    IL2_P607_R IL-2, TCGF, lymphokine cg24372185
    ITK_E166_R EMT, LYK, PSCTK2, MGC126257, MGC126258 cg09489988
    ITK_P114_F EMT, LYK, PSCTK2, MGC126257, MGC126258 cg18953183
    KLK10_P268_R NES1, PRSSL1 cg06130787
    LAT_E46_F LAT1, pp36 cg03108875
    MMP10_E136_R SL-2, STMY2 cg02061229
    MMP2_P303_R CLG4, MONA, CLG4A, TBE-1, MMP-II cg20640526
    MPO_P883_R . cg24997501
    MUSK_P308_F MGC126323, MGC126324 cg22051739
    OPCML_P71_F OPCM, OBCAM cg00738841
    OSM_P188_F MGC20461 cg04546763
    OSM_P34_F MGC20461 cg10467217
    PECAM1_P135_F CD31, PECAM-1 cg05359956
    PGR_E183_R PR, NR3C3 cg24886336
    PSCA_E359_F PRO232 cg20546389
    PTHLH_E251_F HHM, PLP, PTHR, PTHRP, MGC14611 cg01333011
    PTHR1_P258_F PTHR, MGC138426, MGC138452 cg13804333
    PTK6_E50_F BRK cg03004675
    PTK7_E317_F CCK4 cg21726633
    PWCR1_P357_F PET1, HBII-85 cg07197644
    RUNX3_E27_R AML2, CBFA3, PEBP2aC cg21368948
    RUNX3_P247_F AML2, CBFA3, PEBP2aC cg10672665
    RUNX3_P393_R AML2, CBFA3, PEBP2aC cg12607238
    SEMA3B_E96_F SemA, SEMA5, SEMAA, semaV, LUCA-1, FU34863 cg25047248
    SERPINA5_E69_F PCI, PAI3, PROCI, PLANH3 cg08764227
    SHB_P691_R RP11-3J10.8 cg19574087
    SNURF_E256_R . cg07995992
    SNURF_P2_R . cg17916021
    SNURF_P78_F . cg15999943
    SYK_P584_F . cg06713470
    TDG_E129_F . cg09857351
    THBS2_P605_R TSP2 cg24654845
    TNFSF8_E258_R CD153, CD30L, CD30LG cg09980061
    TNFSF8_P184_F CD153, CD30L, CD30LG cg19343707
    ZIM2_P22_F ZNF656 cg01034638
  • TABLE 4B
    Table 4B shows the accession numbers; specific single CpG coordinate;
    presence or absence of CpG islands; specific sequences used in the Illumina
    GoldenGate array experiments; and the synonyms for the genes
    hypermethylated in melanoma. All Accession numbers and location are
    based on Ref. Seq. version 36.1.
    Probe_ID Gid Accession Gene_ID Chrm CpG_Coor Dis_to_TSS CpG_isl
    ALOX12_E85_R 4502050 NM_000697.1 239 17 6840213 85 Y
    ALOX12_P223_R 4502050 NM_000697.1 239 17 6839905 −223 Y
    CDH13_P88_F 61676095 NM_001257.3 1012 16 81217991 −88 Y
    COL1A2_E299_F 48762933 NM_000089.3 1278 7 93862108 299 Y
    DES_E228_R 55749931 NM_001927.3 1674 2 219991571 228 Y
    EPHA2_P203_F 32967310 NM_004431.2 1969 1 16355354 −203 Y
    FRZB_P406_F 38455387 NM_001463.2 2487 2 183440149 −406 Y
    GNMT_P197_F 54792737 NM_018960.4 27232 6 43036281 −197 Y
    GSTM2_P453_R 23065549 NM_000848.2 2946 1 110011761 −453 N
    HOXA11_P698_F 24497552 NM_005523.4 3207 7 27192053 −698 Y
    HPN_P374_R 33695154 NM_182983.1 3249 19 40222876 −374 N
    IPF1_P750_F 4557672 NM_000209.1 3651 13 27391427 −750 Y
    KCNK4_E3_F 15718764 NM_016611.2 50801 11 63815454 3 Y
    LOX_P313_R 21264603 NM_002317.3 4015 5 121442166 −313 Y
    MEST_P62_R 29294638 NM_002402.2 4232 7 129913220 −62 Y
    MST1R_P87_R 4505264 NM_002447.1 4486 3 49916161 −87 Y
    NEFL_E23_R 5453761 NM_006158.1 4747 8 24869923 23 Y
    NPR2_P1093_F 73915098 NM_003995.3 4882 9 35781313 −1093 Y
    RARA_E128_R 75812906 NM_000964.2 5914 17 35719100 128 N
    TNFRSF10D_E27_F 42544227 NM_003840.3 8793 8 23077458 27 Y
    TRIP6_P1090_F 23308730 NM_003302.1 7205 7 100301891 −1090 Y
    TRIP6_P1274_R 23308730 NM_003302.1 7205 7 100301707 −1274 Y
    SEQ
    Probe_ID ID Input_Sequence
    ALOX12_E85_R 54 GGGGCCTGGCTCTTCTCCGGGT[CG]TACAACCGCGTGCAGCTTTGGCTGGTCGG
    ALOX12_P223_R 55 CCGTTGGCCTCACCCTGGCT[CG]GGCCCCTTTATCATCCTGCAGCTACG
    CDH13_P88_F 56 CCGTATCTGCCATGCAAAACGAGGGAG[CG]TTAGGAAGGAATCCGTCTTGTAA
    COL1A2_E299_F 57 ACCCTAGGGCCAGGGAAACTTTTGC[CG]TATAAATAGGGCAGATCCGGGCTTT
    DES_E228_R 58 GGCTCTAAGGGCTCCTCCAGCT[CG]GTGACGTCCCGCGTGTACCAGGTGTC
    EPHA2_P203_F 59 TCCAAAGTTTGAGCGTCTCAAAG[CG]CCAGCGCCCCTACGGATTAGCCC
    FRZB_P406_F 60 GGGACGTCTGTGCCTCTGCCCGGG[CG]GCTCTGCALTTTCCTACCTCCCGC
    GNMT_P197_F 61 GGGATTGCACAGAGGGCTGGGTC[CG]CAGGCTGGCTAAAAGGACCTAGCCC
    GSTM2_P453_R 62 CCTTGCCTGTGTTGTCCTTCCCA[CG]TTAGGTCTGTCATGCCACGTATGTCCGCAG
    HOXA11_P698_F 63 TCATTCATGGTCACTTCCGAAG[CG]CTTTAGTGCCTTCCGTCCCTAAACC
    HPN_P374_R 64 CTCCTTGCTGATTTGCACACATTGGC[CG]CTTCAGACACGCACTTCTGGGGCCA
    IPF1_P750_F 65 CCTCGCTGTATTGGGAAGCTACGTTC[CG]GGCTGGCCAAATGGGCCC
    KCNK4_E3_F 66 GAGATGCCAGATTAGCGTGGTGCCTGTC[CG]GAGAGACGGGCCAGCTGATG
    LOX_P313_R 67 AGGCGAAGGCAGCCAGGCCATGGGG[CG]ACGCCAAAATATGCACGAAGAAAAATG
    MEST_P62_R 68 GCCGGAGGCTATTGTCGAAGCCA[CG]GCCTGCCATTTCATACCCTTTGCAA
    MST1R_P87_R 69 GGACTGGGCCAAATTTAAGCAGCGGTCC[CG]ACAGCCCCAAGATAGCGGACCCCCGCC
    NEFL_E23_R 70 CGCCGCTTGTAGGAGGTCGAGTAGTA[CG]GCTCGTAGCTGAAGGAACTCATG
    NPR2_P1093_F 71 AGGACAAACCCTGGGGTCGCTGG[CG]TGTGTGAGATGGAAATGGA
    RARA_E128_R 72 CCCTTCCCAATTCTTTGGC[CG]CCTTTGACCCCGGCCTCTGCTTCTGA
    TNFRSF10D_E27_F 73 CAGAAATCGTCCCCGTAGTTTGTG[CG]CGTGCAAAGGTTCTCGCAGCTACACTGCCA
    TRIP6_P1090_F 74 AAGGGGACTTTGTGAACAGTGGG[CG]GGGAGACGCAGAGGCAGAGG
    TRIP6_P1274_R 75 CTTGGGCATGGTGCCCGCTTGGCATAG[CG]CCCGGCTCCGGATCTTCCTGTGCCT
    Probe_ID Synonym cg_no
    ALOX12_E85_R LOG12 cg05878700
    ALOX12_P223_R LOG12 cg22819332
    CDH13_P88_F CDHH cg08977371
    COL1A2_E299_F OI4 cg22877867
    DES_E228_R CSM1, CSM2, CMD1I, FLJ12025, FLJ39719, FLJ41013, cg21174728
    FLJ41793
    EPHA2_P203_F ECK cg15146752
    FRZB_P406_F FRE, FZRB, hFIZ, FRITZ, FRP-3, FRZB1, SFRP3, SRFP3, cg25188149
    FRZB-1, FRZB-PEN
    GNMT_P197_F . cg04013093
    GSTM2_P453_R GST4, GSTM, GTHMUS, GSTM2-2 cg11063364
    HOXA11_P698_F HOX1, HOX1I cg17466857
    HPN_P374_R TMPRSS1 cg03537100
    IPF1_P750_F IUF1, PDX1, IDX-1, MODY4, PDX-1, STF-1 cg14584091
    KCNK4_E3_F TRAAK, DKFZP566E164 cg01352108
    LOX_P313_R MGC105112 cg08623535
    MEST_P62_R PEG1, MGC8703, MGC111102, DKFZp686L18234 cg07409197
    MST1R_P87_R RON, PTK8, CDw136 cg01709977
    NEFL_E23_R NFL, NF-L, NF68, CMT1F, CMT2E cg00987688
    NPR2_P1093_F AMDM, NPRB, ANPRB, GUC2B, NPRBi, GUCY2B cg17151902
    RARA_E128_R RAR, NR1B1 cg00848035
    TNFRSF10D_E27_F DCR2, CD264, TRUNDD, TRAILR4 cg01031400
    TRIP6_P1090_F OIP1, ZRP-1, MGC3837, MGC4423, MGC10556, MGC10558, cg09357642
    MGC29959
    TRIP6_P1274_R OIP1, ZRP-1, MGC3837, MGC4423, MGC10556, MGC10558, cg06647679
    MGC29959
    • 6.10. Methylation Profiles for Metastastic Melanoma Samples
  • Using the methods described above, the methylation data for nine melanoma metastases was compared with the benign moles. Eighteen more Genes/CpG sites were found to be significant in this comparison with nine additional hypomethylated and nine hypermethylated genes. The metastases sample descriptions may be found in Table 1. For results of metastases vs. benign nevi see Table 5A and 5B below. For results of combined melanomas and metastases vs. benign nevi see Table 6A and 6B below. For gene descriptions and methylated sequences of the 18 significant additional genes see Table 7A and Table 7B.
  • Table 5A shows the methylation sites, methylation levels, β values for benign nevi and metastatic melanomas and difference in β values for genes hypermethylated in melanoma metastasis.
  • TargetID Met β ave Nevi β ave Met vs Nevi Diff.
    ALOX12_E85_R 0.79 0.33 0.46
    ALOX12_P223_R 0.69 0.41 0.29
    ASCL2_E76_R 0.32 0.11 0.21
    ASCL2_P360_F 0.40 0.10 0.29
    AXIN1_P995_R 0.68 0.31 0.37
    AXL_P223_R 0.47 0.22 0.25
    BCR_P346_F 0.60 0.25 0.35
    CALCA_E174_R 0.53 0.15 0.38
    CCNA1_E7_F 0.26 0.06 0.20
    CD9_P504_F 0.31 0.04 0.27
    CD9_P585_R 0.59 0.19 0.40
    CDH11_E102_R 0.31 0.04 0.28
    CFTR_P372_R 0.55 0.35 0.20
    COL1A2_E299_F 0.58 0.05 0.53
    CTSL_P264_R 0.43 0.18 0.26
    DDIT3_P1313_R 0.60 0.14 0.46
    DES_E228_R 0.29 0.06 0.23
    DIO3_E230_R 0.73 0.51 0.22
    DLK1_E227_R 0.33 0.09 0.24
    DNAJC15_P65_F 0.74 0.53 0.21
    DSC2_E90_F 0.55 0.13 0.42
    EPHA2_P203_F 0.54 0.16 0.38
    EPHA2_P340_R 0.31 0.09 0.22
    EPHA5_P66_F 0.56 0.29 0.27
    ER_seq_a1_S60_F 0.34 0.12 0.23
    ESR2_E66_F 0.34 0.04 0.30
    FASTK_P598_R 0.63 0.39 0.24
    FGF1_E5_F 0.77 0.53 0.24
    FGF1_P357_R 0.75 0.43 0.32
    FRK_P258_F 0.76 0.43 0.33
    FRK_P36_F 0.74 0.40 0.34
    FRZB_E186_R 0.60 0.24 0.35
    FRZB_P406_F 0.47 0.04 0.44
    FZD9_E458_F 0.47 0.25 0.22
    GNMT_E126_F 0.24 0.03 0.21
    GNMT_P197_F 0.47 0.19 0.28
    GRB7_E71_R 0.50 0.28 0.22
    GSTM2_P453_R 0.58 0.21 0.37
    HFE_E273_R 0.36 0.10 0.26
    HOXA5_E187_F 0.82 0.58 0.24
    HOXA5_P1324_F 0.57 0.34 0.23
    HOXA9_E252_R 0.71 0.27 0.43
    HS3ST2_E145_R 0.41 0.06 0.35
    IGF1_E394_F 0.74 0.34 0.40
    IGF2AS_P203_F 0.45 0.20 0.25
    IGFBP5_P9_R 0.36 0.14 0.21
    IHH_E186_F 0.29 0.06 0.24
    IL17RB_E164_R 0.26 0.06 0.20
    IPF1_P750_F 0.64 0.38 0.26
    KCNK4_E3_F 0.43 0.09 0.34
    LIG3_P622_R 0.57 0.32 0.25
    LOX_P313_R 0.47 0.09 0.39
    LYN_P241_F 0.30 0.06 0.24
    MAP3K8_P1036_F 0.77 0.28 0.49
    MC2R_P1025_F 0.47 0.22 0.25
    MOS_E60_R 0.33 0.13 0.20
    MST1R_E42_R 0.83 0.62 0.21
    MST1R_P87_R 0.83 0.38 0.46
    MT1A_E13_R 0.39 0.17 0.22
    MYOD1_E156_F 0.45 0.04 0.41
    NEFL_E23_R 0.50 0.24 0.26
    NEO1_P1067_F 0.34 0.06 0.28
    NPR2_P1093_F 0.88 0.57 0.31
    NPR2_P618_F 0.30 0.08 0.22
    OGG1_E400_F 0.45 0.06 0.39
    p16_seq_47_S188_R 0.24 0.04 0.20
    PAX6_P1121_F 0.34 0.10 0.24
    PENK_P447_R 0.33 0.09 0.24
    PGF_P320_F 0.36 0.06 0.29
    PYCARD_P393_F 0.28 0.08 0.21
    RARA_E128_R 0.36 0.11 0.25
    RARA_P176_R 0.65 0.37 0.28
    RARB_P60_F 0.40 0.12 0.28
    RARRES1_P426_R 0.66 0.42 0.24
    RIPK3_P124_F 0.51 0.27 0.24
    S100A4_E315_F 0.38 0.11 0.28
    SEMA3A_P658_R 0.51 0.30 0.21
    SEPT5_P441_F 0.40 0.14 0.26
    SEPT5_P464_R 0.59 0.30 0.28
    SEPT9_P58_R 0.62 0.18 0.44
    SOX17_P287_R 0.49 0.23 0.26
    SOX17_P303_F 0.39 0.17 0.23
    SOX2_P546_F 0.39 0.10 0.29
    TAL1_E122_F 0.35 0.14 0.20
    TGFB2_E226_R 0.50 0.29 0.21
    TGFBI_P173_F 0.45 0.22 0.24
    TNFRSF10C_P7_F 0.38 0.14 0.24
    TNFRSF10D_E27_F 0.69 0.42 0.27
    TNK1_P221_F 0.51 0.15 0.36
    TRIP6_P1090_F 0.64 0.11 0.53
    TRIP6_P1274_R 0.69 0.22 0.47

    Table 5B shows the methylation sites, methylation levels, β values for benign nevi and metastatic melanomas and difference in β values for genes hypomethylated in melanoma metastasis.
  • TargetID Met β ave Nevi β ave Met vs Nevi
    AFF3_P122_F 0.71 0.98 −0.26
    ATP10A_P524_R 0.59 0.83 −0.24
    BCL3_E71_F 0.21 0.42 −0.21
    CAPG_E228_F 0.52 0.75 −0.23
    CASP8_E474_F 0.40 0.75 −0.36
    CCL3_E53_R 0.62 0.93 −0.31
    CD2_P68_F 0.57 0.96 −0.39
    CD34_P780_R 0.58 0.88 −0.30
    CD86_P3_F 0.41 0.76 −0.35
    COL1A1_P117_R 0.31 0.68 −0.36
    DLC1_P695_F 0.70 0.94 −0.24
    DNASE1L1_P39_R 0.26 0.54 −0.28
    EMR3_E61_F 0.50 0.89 −0.39
    EMR3_P39_R 0.47 0.90 −0.43
    EVI2A_E420_F 0.65 0.97 −0.32
    EVI2A_P94_R 0.33 0.77 −0.44
    GUCY2D_P48_R 0.26 0.49 −0.22
    HLA-DOA_P191_R 0.60 0.81 −0.21
    HLA-DPA1_P28_R 0.42 0.89 −0.47
    HLA-DPB1_E2_R 0.31 0.71 −0.41
    HLA-DRA_P77_R 0.13 0.41 −0.29
    IFNG_P459_R 0.62 0.90 −0.28
    IL1B_P829_F 0.52 0.73 −0.21
    1L2_P607_R 0.68 0.89 −0.22
    ITK_E166_R 0.71 0.97 −0.27
    ITK_P114_F 0.63 0.92 −0.29
    KLK10_P268_R 0.18 0.67 −0.49
    KRT1_P798_R 0.64 0.85 −0.22
    LAT_E46_F 0.34 0.89 −0.56
    LTA_P214_R 0.65 0.94 −0.30
    LTB4R_P163_F 0.76 0.96 −0.20
    MMP10_E136_R 0.70 0.91 −0.21
    MMP2_P197_F 0.18 0.64 −0.46
    MMP2_P303_R 0.31 0.83 −0.51
    MMP7_E59_F 0.40 0.61 −0.21
    MPO_P883_R 0.16 0.76 −0.60
    MT1A_P600_F 0.68 0.95 −0.27
    MUSK_P308_F 0.69 0.91 −0.22
    NOTCH4_P938_F 0.65 0.94 −0.29
    OPCML_P71_F 0.27 0.71 −0.44
    OSM_P188_F 0.61 0.96 −0.36
    OSM_P34_F 0.55 0.91 −0.36
    PECAM1_P135_F 0.71 0.94 −0.23
    PLAU_P176_R 0.27 0.49 −0.22
    POMC_P400_R 0.60 0.87 −0.27
    PSCA_E359_F 0.52 0.85 −0.33
    PTHLH_E251_F 0.58 0.91 −0.33
    PTHR1_P258_F 0.47 0.83 −0.36
    PTK6_E50_F 0.36 0.61 −0.25
    PTPN6_E171_R 0.51 0.90 −0.39
    PTPN6_P282_R 0.71 0.95 −0.23
    RUNX3_E27_R 0.58 0.96 −0.37
    RUNX3_P247_F 0.60 0.96 −0.36
    RUNX3_P393_R 0.72 0.96 −0.24
    S100A4_P194_R 0.70 0.90 −0.20
    SEMA3B_E96_F 0.21 0.68 −0.47
    SEMA3B_P110_R 0.25 0.69 −0.44
    SEMA3C_P642_F 0.45 0.70 −0.25
    SERPINA5_P156_F 0.25 0.47 −0.22
    SHB_P691_R 0.33 0.80 −0.47
    SLC14A1_E295_F 0.70 0.92 −0.22
    SNURF_E256_R 0.64 0.85 −0.21
    SPDEF_E116_R 0.40 0.70 −0.31
    SPI1_P48_F 0.74 0.97 −0.23
    TDGF1_E53_R 0.59 0.82 −0.22
    THBS2_P605_R 0.46 0.93 −0.46
    TIE1_E66_R 0.73 0.96 −0.23
    TNFSF10_E53_F 0.36 0.67 −0.30
    TNFSF10_P2_R 0.55 0.91 −0.35
    TNFSF8_E258_R 0.59 0.95 −0.36
    TNFSF8_P184_F 0.18 0.50 −0.32
    VAMP8_P114_F 0.31 0.67 −0.37
    ZAP70_P220_R 0.63 0.89 −0.26

    Table 6 shows the methylation sites, Raw β values, Bonferroni corrections, methylation levels, β values for benign nevi and combined melanomas and metastatic melanomas and difference in β values. A positive meandif shows hypomethylation in melanoma and a negative meandif is hypermethylation in melanoma.
  • TargetID Raw_p Bonferroni_p FDR_p Mel_Mean Mol_Mean Meandif
    ACTG2_P346_F 1.82E−09 1.73E−06 2.83E−08 0.762 0.915 0.154
    ACVR1_E328_R 7.08E−06 0.00671794 4.1E−05 0.763 0.891 0.127
    AFF3_P122_F 5.59E−13 5.31E−10 2.53E−11 0.815 0.977 0.162
    AGXT_E115_R 1.58E−09 1.50E−06 2.58E−08 0.921 0.969 0.049
    ALOX12_E85_R 5.65E−10 5.36E−07 1.12E−08 0.775 0.322 −0.452
    ALOX12_P223_R 4.33E−06 0.00411105 2.69E−05 0.718 0.411 −0.307
    APBA2_P227_F 8.17E−11 7.76E−08 2.22E−09 0.918 0.981 0.063
    APBA2_P305_R 3.94E−06 0.0037405 2.52E−05 0.845 0.932 0.087
    ARHGAP9_P260_F 5.23E−05 0.04967831 0.000248 0.828 0.945 0.117
    ARHGDIB_P148_R 7.36E−08 6.9888E−05 6.59E−07 0.406 0.613 0.207
    B3GALT5_P330_F 4.10E−08 3.8934E−05 4.01E−07 0.821 0.956 0.135
    BCL3_E71_F 6.56E−08 6.2267E−05 5.99E−07 0.217 0.415 0.199
    BLK_P668_R 1.12E−12 1.07E−09 4.84E−11 0.857 0.971 0.114
    BMPR1A_E88_F 2.78E−07 0.00026391 2.26E−06 0.537 0.766 0.229
    BMPR2_P1271_F 9.25E−06 0.00877848 5.19E−05 0.031 0.065 0.034
    C4B_P191_F 7.36E−08 6.9888E−05 6.59E−07 0.923 0.976 0.053
    CARD15_P302_R 5.18E−06 0.00491922 3.13E−05 0.250 0.537 0.286
    CASP8_E474_F 5.47E−09 5.19E−06 7.53E−08 0.390 0.750 0.360
    CCL3_E53_R 2.07E−13 1.96E−10 1.09E−11 0.678 0.927 0.249
    CD1A_P414_R 2.24E−08 2.1257E−05 2.42E−07 0.894 0.977 0.084
    CD2_P68_F 1.52E−16 1.45E−13 2.89E−14 0.669 0.960 0.291
    CD34_P339_R 7.60E−10 7.21E−07 1.44E−08 0.753 0.909 0.156
    CD34_P780_R 3.96E−06 0.00375531 2.52E−05 0.668 0.880 0.212
    CD86_P3_F 1.16E−06 0.00110267 8.17E−06 0.421 0.757 0.336
    CDH11_E102_R 6.19E−06 0.00587433 3.65E−05 0.351 0.036 −0.315
    CDH13_P88_F 4.64E−06 0.00440444 2.86E−05 0.666 0.367 −0.299
    CDH17_P376_F 5.84E−08 5.5435E−05 5.38E−07 0.906 0.959 0.053
    COL1A1_P117_R 1.05E−08 9.99E−06 1.31E−07 0.342 0.677 0.335
    COL1A2_E299_F 8.13E−09 7.71E−06 1.06E−07 0.614 0.051 −0.563
    COMT_E401_F 2.8E−05 0.02660434 0.000142 0.122 0.232 0.111
    CSF2_E248_R 4.11E−12 3.90E−09 1.56E−10 0.880 0.969 0.088
    CSF3_E242_R 3.18E−09 3.02E−06 4.65E−08 0.914 0.970 0.056
    CSF3_P309_R 4.83E−10 4.58E−07 9.96E−09 0.775 0.907 0.132
    DES_E228_R 3.03E−10 2.87E−07 6.68E−09 0.283 0.063 −0.220
    DES_P1006_R 4.79E−09 4.54E−06 6.78E−08 0.740 0.887 0.148
    DLC1_P695_F 2.70E−12 2.56E−09 1.07E−10 0.731 0.941 0.210
    DMP1_P134_F 7.13E−09 6.77E−06 9.53E−08 0.824 0.940 0.116
    DSC2_E90_F 4.33E−06 0.00411105 2.69E−05 0.400 0.129 −0.271
    DSG1_E292_F 1.73E−06 0.00163847 1.18E−05 0.683 0.896 0.213
    DSG1_P159_R 3.04E−05 0.02880779 0.000151 0.394 0.663 0.270
    EGF_P242_R 2.59E−10 2.45E−07 5.98E−09 0.843 0.951 0.108
    EGR4_E70_F 1.05E−06 0.00099955 7.57E−06 0.223 0.366 0.143
    EMR3_E61_F 8.82E−10 8.37E−07 1.61E−08 0.501 0.889 0.388
    EMR3_P39_R 1.08E−10 1.03E−07 2.78E−09 0.604 0.900 0.296
    EPHA2_P203_F 4.10E−08 3.8934E−05 4.01E−07 0.515 0.162 −0.353
    EPHA2_P340_R 1.71E−06 0.00162373 1.18E−05 0.335 0.090 −0.245
    EPHB4_P313_R 5.65E−06 0.00536546 3.38E−05 0.071 0.184 0.113
    EPHX1_P22_F 4.07E−11 3.87E−08 1.25E−09 0.897 0.968 0.071
    ERBB3_E331_F 3.84E−05 0.03647948 0.000189 0.056 0.081 0.025
    EVI2A_E420_F 9.23E−14 8.76E−11 6.26E−12 0.727 0.966 0.239
    EVI2A_P94_R 1.79E−11 1.70E−08 6.30E−10 0.311 0.764 0.453
    FER_E119_F 2.39E−05 0.02266018 0.000122 0.062 0.149 0.087
    FGF6_P139_R 4.23E−05 0.0401189 0.000205 0.799 0.948 0.148
    FGF7_P610_F 4.16E−05 0.03943251 0.000202 0.898 0.951 0.053
    FGF9_P1404_F 5.67E−06 0.00537696 3.38E−05 0.103 0.170 0.068
    FGFR1_E317_F 3.96E−06 0.00375531 2.52E−05 0.063 0.109 0.045
    FGR_P39_F 8.77E−06 0.00832709 4.96E−05 0.942 0.973 0.031
    FOSL2_E384_R 2.24E−08 2.1257E−05 2.42E−07 0.892 0.953 0.061
    FRZB_P406_F 1.62E−09 1.53E−06 2.60E−08 0.481 0.036 −0.445
    FZD9_P175_F 7.07E−07 0.00067093 5.24E−06 0.138 0.201 0.063
    GABRA5_P1016_F 7.60E−10 7.21E−07 1.44E−08 0.763 0.955 0.192
    GNMT_P197_F 2.78E−07 0.00026391 2.26E−06 0.483 0.189 −0.294
    GPR116_E328_R 2.50E−07 0.00023715 2.06E−06 0.896 0.968 0.072
    GPR116_P850_F 1.79E−08 1.6964E−05 2.07E−07 0.868 0.934 0.067
    GSTM2_P453_R 7.94E−10 7.53E−07 1.48E−08 0.577 0.202 −0.374
    HBII-52_P563_F 6.76E−06 0.00641451 3.94E−05 0.579 0.865 0.286
    HBII-52_P659_F 2.35E−06 0.00222931 1.57E−05 0.827 0.957 0.130
    HGF_P1293_R 5.21E−07 0.00049439 3.96E−06 0.911 0.968 0.057
    HLA-DPA1_P28_R 4.83E−10 4.58E−07 9.96E−09 0.516 0.884 0.367
    HLA-DPB1_P540_F 1.20E−08 1.1358E−05 1.48E−07 0.948 0.980 0.032
    HOXA11_P698_F 1.56E−05 0.01478451 8.31E−05 0.863 0.674 −0.189
    HOXA9_E252_R 7.38E−07 0.00070047 5.43E−06 0.732 0.288 −0.444
    HTR2A_E10_R 4.74E−06 0.00449816 2.88E−05 0.849 0.946 0.096
    IAPP_E280_F 1.34E−08 1.2717E−05 1.63E−07 0.837 0.952 0.115
    ICAM1_E242_F 1.72E−05 0.0163513 9.08E−05 0.048 0.090 0.043
    IFNG_P459_R 2.36E−11 2.24E−08 8.01E−10 0.641 0.898 0.257
    IGF1_E394_F 2.46E−07 0.00023381 2.05E−06 0.645 0.343 −0.302
    IGF2AS_E4_F 1.05E−06 0.00099955 7.57E−06 0.164 0.311 0.147
    IL10_P348_F 9.23E−14 8.76E−11 6.26E−12 0.945 0.982 0.037
    IL12B_E25_F 3.72E−06 0.00353231 2.42E−05 0.896 0.948 0.052
    IL12B_P1453_F 2.2E−05 0.02089918 0.000114 0.758 0.874 0.115
    IL13_E75_R 1.88E−10 1.78E−07 4.45E−09 0.931 0.980 0.049
    IL2_P607_R 3.68E−11 3.49E−08 1.20E−09 0.585 0.893 0.308
    IPF1_P750_F 1.05E−06 0.00099955 7.57E−06 0.700 0.372 −0.328
    ITK_E166_R 1.06E−14 1.00E−11 1.00E−12 0.754 0.974 0.221
    ITK_P114_F 2.07E−13 1.96E−10 1.09E−11 0.624 0.919 0.295
    JAG1_P66_F 2.2E−05 0.02089918 0.000114 0.064 0.113 0.049
    KCNK4_E3_F 3.03E−10 2.87E−07 6.68E−09 0.457 0.093 −0.364
    KLK10_P268_R 3.54E−10 3.36E−07 7.64E−09 0.246 0.664 0.418
    KLK11_P1290_F 2.86E−08 2.7146E−05 2.92E−07 0.827 0.944 0.118
    KRT1_P798_R 1.09E−09 1.03E−06 1.88E−08 0.663 0.851 0.188
    LAT_E46_F 5.00E−13 4.74E−10 2.50E−11 0.487 0.893 0.406
    LCK_E28_F 2.84E−14 2.70E−11 2.25E−12 0.798 0.956 0.159
    LMO2_E148_F 1.22E−13 1.15E−10 7.22E−12 0.895 0.977 0.082
    LOX_P313_R 4.02E−07 0.00038107 3.15E−06 0.524 0.085 −0.439
    LTA_P214_R 1.35E−10 1.28E−07 3.38E−09 0.723 0.943 0.220
    LTB4R_P163_F 3.43E−15 3.25E−12 4.07E−13 0.818 0.962 0.144
    MAP3K8_P1036_F 1.16E−06 0.00110267 8.17E−06 0.605 0.277 −0.327
    MAPK9_P1175_F 3.89E−05 0.03695243 0.00019 0.919 0.963 0.044
    MAS1_P469_R 3.66E−08 3.4691E−05 3.69E−07 0.904 0.962 0.058
    MAS1_P657_R 5.20E−08 4.9315E−05 4.98E−07 0.923 0.975 0.053
    MEST_P62_R 1.04E−05 0.00988532 5.68E−05 0.586 0.287 −0.299
    MMP10_E136_R 1.18E−09 1.12E−06 2.00E−08 0.690 0.914 0.223
    MMP19_E274_R 2.74E−06 0.00260103 1.81E−05 0.839 0.934 0.095
    MMP2_P197_F 1.81E−07 0.00017139 1.54E−06 0.296 0.648 0.352
    MMP2_P303_R 1.02E−09 9.70E−07 1.80E−08 0.431 0.829 0.398
    MMP7_P613_F 4.86E−11 4.61E−08 1.40E−09 0.885 0.958 0.073
    MMP9_P237_R 1.7E−05 0.01609838 8.99E−05 0.075 0.148 0.073
    MPL_P62_F 1.25E−09 1.19E−06 2.08E−08 0.828 0.950 0.122
    MPO_P883_R 1.52E−16 1.45E−13 2.89E−14 0.209 0.762 0.553
    MSH3_E3_F 1.16E−07 0.00011008 1.00E−06 0.772 0.875 0.103
    MSH3_P13_R 2.39E−05 0.02266018 0.000122 0.546 0.690 0.144
    MST1R_P87_R 5.84E−08 5.5435E−05 5.38E−07 0.704 0.369 −0.335
    MT1A_P600_F 1.28E−06 0.00121572 8.94E−06 0.736 0.954 0.218
    MUSK_P308_F 2.21E−08 2.1012E−05 2.42E−07 0.662 0.908 0.246
    MYOD1_E156_F 1.56E−06 0.00148455 1.08E−05 0.277 0.043 −0.234
    NEFL_E23_R 1.04E−05 0.00988532 5.68E−05 0.499 0.243 −0.256
    NOS2A_E117_R 5.04E−12 4.79E−09 1.84E−10 0.849 0.962 0.113
    NOTCH4_P938_F 1.75E−08 1.6587E−05 2.05E−07 0.732 0.936 0.204
    NPR2_P1093_F 7.55E−08 7.1693E−05 6.70E−07 0.817 0.578 −0.239
    OPCML_P71_F 4.10E−07 0.00038891 3.19E−06 0.278 0.711 0.432
    OSM_P188_F 3.05E−16 2.89E−13 4.82E−14 0.696 0.963 0.267
    OSM_P34_F 1.08E−10 1.03E−07 2.78E−09 0.630 0.913 0.283
    PDGFA_P78_F 3.04E−05 0.02880779 0.000151 0.104 0.170 0.065
    PDGFRA_E125_F 1.2E−05 0.01141812 6.49E−05 0.776 0.928 0.152
    PECAM1_P135_F 1.22E−13 1.15E−10 7.22E−12 0.722 0.938 0.217
    PGR_E183_R 5.23E−05 0.04967831 0.000248 0.665 0.840 0.175
    PIK3R1_P307_F 1.1E−05 0.01046542 5.98E−05 0.907 0.955 0.047
    PLA2G2A_E268_F 5.84E−08 5.5435E−05 5.38E−07 0.721 0.899 0.178
    PLG_E406_F 4.86E−11 4.61E−08 1.40E−09 0.810 0.947 0.137
    PMP22_P975_F 5.91E−09 5.61E−06 8.01E−08 0.783 0.952 0.169
    PRDM2_P1340_R 4.69E−05 0.04451017 0.000225 0.914 0.960 0.047
    PROM1_P44_R 1.81E−10 1.72E−07 4.40E−09 0.834 0.954 0.120
    PSCA_E359_F 2.24E−08 2.1257E−05 2.42E−07 0.600 0.847 0.247
    PTHLH_E251_F 2.70E−12 2.56E−09 1.07E−10 0.613 0.909 0.296
    PTHLH_P757_F 1.49E−14 1.41E−11 1.28E−12 0.844 0.955 0.111
    PTHR1_E36_R 1.01E−08 9.63E−06 1.28E−07 0.924 0.966 0.042
    PTHR1_P258_F 8.13E−09 7.71E−06 1.06E−07 0.540 0.831 0.291
    PTK6_E50_F 1.88E−06 0.00178615 1.28E−05 0.302 0.617 0.314
    PTK7_E317_F 2.86E−08 2.7146E−05 2.92E−07 0.424 0.668 0.245
    PTPN6_E171_R 3.02E−05 0.02869854 0.000151 0.670 0.898 0.227
    PTPN6_P282_R 1.91E−05 0.01814096 9.97E−05 0.855 0.946 0.091
    PWCR1_E81_R 2.77E−09 2.63E−06 4.11E−08 0.858 0.974 0.116
    PWCR1_P357_F 3.30E−06 0.00312863 2.16E−05 0.663 0.858 0.194
    PYCARD_P393_F 1.16E−06 0.00110267 8.17E−06 0.287 0.077 −0.210
    RARA_E128_R 4.33E−06 0.00411105 2.69E−05 0.368 0.108 −0.261
    RIPK3_P124_F 8.47E−06 0.00803373 4.81E−05 0.613 0.272 −0.341
    RUNX3_E27_R 1.06E−14 1.00E−11 1.00E−12 0.611 0.958 0.346
    RUNX3_P247_F 1.43E−16 1.35E−13 2.89E−14 0.584 0.965 0.380
    RUNX3_P393_R 1.52E−16 1.45E−13 2.89E−14 0.705 0.963 0.257
    S100A4_E315_F 9.56E−06 0.009075 5.31E−05 0.377 0.105 −0.272
    SEMA3B_E96_F 4.62E−08 4.3835E−05 4.47E−07 0.333 0.685 0.351
    SERPINA5_E69_F 7.38E−06 0.00700089 4.22E−05 0.595 0.787 0.191
    SFTPA1_P421_F 9.00E−10 8.54E−07 1.61E−08 0.806 0.940 0.134
    SFTPB_P689_R 2.97E−07 0.00028206 2.37E−06 0.758 0.885 0.127
    SFTPD_E169_F 9.26E−09 8.78E−06 1.19E−07 0.781 0.936 0.155
    SHB_P691_R 1.36E−08 1.2898E−05 1.63E−07 0.430 0.805 0.376
    SLC14A1_E295_F 2.10E−09 1.99E−06 3.21E−08 0.729 0.917 0.188
    SLC22A2_E271_R 2.85E−08 2.7048E−05 2.92E−07 0.926 0.976 0.050
    SLC22A3_P634_F 4.74E−06 0.00449816 2.88E−05 0.636 0.816 0.181
    SNCG_P98_R 9.56E−06 0.009075 5.31E−05 0.707 0.866 0.158
    SNRPN_SEQ_18_S99_F 4.22E−06 0.00400335 2.67E−05 0.642 0.792 0.150
    SNURF_E256_R 2.85E−08 2.7048E−05 2.92E−07 0.591 0.849 0.258
    SNURF_P2_R 4.18E−09 3.97E−06 6.01E−08 0.412 0.613 0.200
    SNURF_P78_F 2.74E−06 0.00260103 1.81E−05 0.636 0.805 0.169
    SOD3_P225_F 3.96E−11 3.76E−08 1.25E−09 0.946 0.980 0.033
    SPI1_E205_F 6.76E−06 0.00641451 3.94E−05 0.543 0.715 0.171
    SPI1_P48_F 7.62E−17 7.23E−14 2.89E−14 0.797 0.969 0.172
    STAT5A_E42_F 9.26E−08 8.7841E−05 8.06E−07 0.093 0.205 0.112
    SYK_P584_F 4.24E−07 0.00040208 3.27E−06 0.707 0.896 0.189
    TDGF1_E53_R 3.09E−07 0.00029349 2.45E−06 0.627 0.815 0.189
    TDG_E129_F 5.84E−08 5.5435E−05 5.38E−07 0.638 0.818 0.180
    TEK_P526_F 2.27E−06 0.00215777 1.53E−05 0.695 0.856 0.162
    TFF2_P557_R 2.53E−08 2.4032E−05 2.70E−07 0.910 0.974 0.065
    THBS2_P605_R 1.95E−08 1.8488E−05 2.23E−07 0.573 0.944 0.370
    THPO_E483_F 5.47E−09 5.19E−06 7.53E−08 0.915 0.976 0.061
    TIE1_E66_R 5.59E−13 5.31E−10 2.53E−11 0.774 0.957 0.183
    TIMP3_P690_R 5.21E−07 0.00049439 3.96E−06 0.961 0.982 0.021
    TJP2_P518_F 2.59E−05 0.02455862 0.000131 0.176 0.335 0.159
    TNFRSF10D_E27_F 1.04E−05 0.00988532 5.68E−05 0.721 0.411 −0.309
    TNFSF10_E53_F 1.87E−05 0.01775313 9.81E−05 0.374 0.669 0.294
    TNFSF8_E258_R 5.33E−16 5.06E−13 7.23E−14 0.585 0.950 0.365
    TNFSF8_P184_F 4.10E−08 3.8934E−05 4.01E−07 0.225 0.497 0.272
    TRAF4_P372_F 1.98E−08 1.8786E−05 2.24E−07 0.142 0.314 0.172
    TRIP6_P1090_F 9.26E−08 8.7841E−05 8.06E−07 0.598 0.116 −0.482
    TRIP6_P1274_R 1.54E−08 1.4634E−05 1.83E−07 0.652 0.224 −0.428
    TRPM5_E87_F 5.79E−11 5.50E−08 1.62E−09 0.790 0.938 0.148
    UGT1A1_E11_F 6.39E−07 0.00060637 4.77E−06 0.932 0.976 0.045
    UGT1A1_P315 R 6.19E−06 0.00587433 3.65E−05 0.699 0.852 0.153
    UGT1A1_P564 R 3.84E−05 0.03647948 0.000189 0.942 0.980 0.039
    USP29_P282_R 7.38E−06 0.00700089 4.22E−05 0.845 0.954 0.109
    VAMP8_P114_F 4.49E−05 0.04260645 0.000216 0.398 0.673 0.275
    VAV2_P1182_F 2.91E−07 0.00027589 2.34E−06 0.035 0.060 0.025
    WNT8B_E487_F 5.02E−10 4.76E−07 1.01E−08 0.767 0.924 0.156
    WNT8B_P216_R 2.12E−07 0.00020104 1.78E−06 0.920 0.954 0.034
    XPC_P226_R 5.77E−07 0.0005477 4.35E−06 0.731 0.865 0.134
    ZAP70_P220_R 1.32E−05 0.01249291 7.06E−05 0.728 0.894 0.166
    ZIM2_P22_F 2.01E−07 0.00019112 1.71E−06 0.536 0.721 0.186
    ZIM3_E203_F 2.77E−09 2.63E−06 4.11E−08 0.916 0.979 0.063
    ZNFN1A1_P179_F 1.64E−09 1.56E−06 2.60E−08 0.933 0.980 0.048
  • TABLE 7A
    Table 7A shows the accession numbers; specific single CpG coordinate;
    presence or absence of CpG islands; specific sequences used in the
    Illumina GoldenGate array experiments; and the synonyms for additional
    genes hypomethylated in melanoma metastasis.
    All Accession numbers and location are based on Ref. Seq. version 36.1.
    Probe_ID Gid Accession Gene_ID Chrm CpG_Coor Dis_to_TSS CpG I
    CD34_P780_R 68342037 NM_001025109.1 947 1 206152086 −780 N
    DLC1_P695_F 33188432 NM_182643.1 10395 8 13417461 −695 N
    LTA_P214_R 6806892 NM_000595.2 4049 6 31647858 −214 N
    MMP2_P197_F 75905807 NM_004530.2 4313 16 54070392 −197 Y
    MT1A_P600_F 71274112 NM_005946.2 4489 16 55229479 −600 Y
    NOTCH4_P938_F 55770875 NM_004557.3 4855 6 32300760 −938 N
    PTPN6_E171_R 34328901 NM_080548.2 5777 12 6926172 171 Y
    TNFSF10_E53_F 23510439 NM_003810.2 8743 3 173723910 53 N
    VAMP8_P114_F 14043025 NM_003761.2 8673 2 85658114 −114 N
    SEQ
    Probe_ID ID Input_Sequence
    CD34_P780_R 76 GGCAGCCTAGTCTTGGGGACGTAGAGA[CG]GGAGAAAGGAGAAGCCAGCCT
    DLC1_P695_F 77 ACAACTGCTTCCATCTAGCATGGCAG[CG]TTCCTGAATCACATCTCTAAAGCCGCT
    LTA_P214_R 78 CCTTTCCCAGAACTCAGT[CG]CCTGAACCCCCAGCCTGTGGTTCTC
    MMP2_P197_F 79 GCGAGAGAGGCAAGTGGGGTGA[CG]AGGTCGTGCACTGAGGGTG
    MT1A_P600_F
    80 AGAGTGAGAGGCCGACCCGTGTTCC[CG]TGTTACTGTGTACGGAGTAGTGG
    NOTCH4_P938_F 81 CCTGAGAGCCTTCCCCTAC[CG]GGGAATATACTTCACCAGCACCACTTT
    PTPN6_E171_R 82 GAGATGCTGTCCCGTGGGTAAGTCC[CG]GGCACCATCGGGGTCCCAGTCT
    TNFSF10_E53_F 83 GACTGCTGTAAGTCAGCCAGGCAGC[CG]GTCACTGAAGCCCTTCCTTCTCTATT
    VAMP8_P114_F 84 CACTGGGAGGACAGTGAAGAATGCC[CG]CCTACCTGGGGAAACCTGAGT
    Probe_ID Synonym cg_no
    CD34_P780_R . cg14637677
    DLC1_P695_F HP, ARHGAP7, STARD12, FLJ21120, p122-RhoGAP cg00933411
    LTA_P214_R LT, TNFB, TNFSF1 cg20798246
    MMP2_P197_F CLG4, MONA, CLG4A, TBE-1, MMP-II cg20597545
    MT1A_P600_F MT1, MTC, MT1S, MGC32848 cg10731123
    NOTCH4_P938_F INT3, NOTCH3, MGC74442 cg05166027
    PTPN6_E171_R HCP, HCPH, SHP1, SHP-1, HPTP1C, PTP-1C, SHP-1L, cg00788854
    SH-PTP1
    TNFSF10_E53_F TL2, APO2L, CD253, TRAIL, Apo-2L cg16555388
    VAMP8_P114_F EDB, VAMP5 cg17641218
  • TABLE 7B
    Table 7B shows the accession numbers; specific single CpG coordinate;
    presence or absence of CpG islands; specific sequences used in the
    Illumina GoldenGate array experiments; and the synonyms for additional
    genes hypermethylated in melanoma metastasis. All Accession numbers
    and location are based on Ref. Seq. version 36.1.
    Probe_ID Gid Accession Ge_ID Chrm CpG_Coor Dis_to_TS CpG_i
    IGF1_E394_F 19923111 NM_000618.2 3479 12 101398060 394 N
    HOXA9_E252_R 24497558 NM_002142.3 3205 7 27171422 252 Y
    MAP3K8_P1036_F 22035597 NM_005204.2 1326 10 30761836 −1036 Y
    PYCARD_P393_F 22035619 NM_145182.1 29108 16 31122145 −393 N
    MYOD1_E156_F 23111008 NM_002478.3 4654 11 17697891 156 Y
    DSC2_E90_F 40806177 NM_024422.2 1824 18 26936285 90 Y
    CDH11_E102_R 16306531 NM_001797.2 1009 16 63713318 102 Y
    RIPK3_P124_F 40254843 NM_006871.2 11035 14 23879137 −124 N
    S100A4_E315_F 9845515 NM_019554.1 6275 1 151784591 315 N
    Probe_ID SEQ ID Input_Sequence
    IGF1_E394_F 85 TGTGCAAATGCATCCATCTCCC[CG]AGCTATTTTTCAGATTCCACAGAATTGCA
    HOXA9_E252_R 86 TGGGTTCCACGAGGCGCCAAACACCGT[CG]CCTTGGACTGGAAGCTGCACG
    MAP3K8_P1036_F 87 ACCTGGGCACTGGGAAGAATAGGG[CG]TGGACTTGGAGTGTGACCG
    PYCARD_P393_F 88 CCAGCATAACATGGCCAACC[CG]ATGGCTCCCGAAACCTTGCCAGATGC
    MYOD1_E156_F 89 TGGGCGAAGCCAGGACCGTGCCG[CG]CCACCGCCAGGATATGGAGCTACTGTC
    DSC2_E90_F 90 CTGCGCAAGGTGTTTCTCACCAG[CG]GACGCCACCTATAAGGCCCATCTC
    CDH11_E102_R 91 GAGGGTGGACGCAACCTCCGAGC[CG]CCAGTCCCTGGCGCAGGGCAAGCG
    RIPK3_P124_F 92 AAAGCTAGTGCCTTTCTCCTTGACTAG[CG]TTTCCTGAGCACCTGCCGCAGCC
    S100A4_E315_F 93 CATACCAACACGTACTATAGCAACAG[CG]TGTGCAAGCCCACATCTCAGAAGCA
    Probe_ID Synonym cg_no
    IGF1_E394_F IGFI cg17084217
    HOXA9_E252_R HOX1, ABD-B, HOX1G, HOX1.7, MGC1934 cg10604830
    MAP3K8_P1036_F COT, EST, ESTF, TPL2, Tpl-2, c-COT, FLJ10486 cg21555918
    PYCARD_P393_F ASC, TMS1, CARD5, MGC10332 cg23185156
    MYOD1_E156_F PUM, MYF3, MYOD cg20325846
    DSC2_E90_F DG2, DSC3, CDHF2, DGII/III, DKFZp686I11137 cg08156793
    CDH11_E102_R OB, CAD11, CDHOB, OSF-4 cg05318914
    RIPK3_P124_F RIP3, RIP3 beta, RIP3 gamma cg13583230
    S100A4_E315_F 42A, 18A2, CAPL, MTS1, P9KA, PEL98 cg22502265
  • The results above were confirmed in a second sample set. Specifically, sample set #2, an independent set of 25 melanomas and 29 nevi underwent DNA methylation profiling using the Illumina GoldenGate Cancer Panel I and passed filtering criteria. The melanomas were of a variety of histologic subtypes and ranged in Breslow thickness from 0.42 to 10.75 mm. The majority of nevi (21 of 29) had varying degree of histologic atypia. Of the panel of 22 genes identified through analysis of the initial sample set, 14 were also statistically significant for differential methylation in an independent data set including dysplastic nevi after adjustment for age, sex and multiple comparisons. In order to identify and account for potential confounders in studying methylation differences between melanomas and nevi, host factors such as age, sex, anatomic site, and solar elastosis (sun damage to the surrounding lesional skin) were examined. These host factors were not associated with differential methylation at the 26 loci in the marker panel.
  • The 14 genes were CARD15, CD2, EMR3 (2 CpG loci), EVI2A, FRZB, HLA-DPA1, IFNG, IL2, ITK, LAT, MPO, PTHLH, RUNX3 (3 CpG loci), and TNFSF8. It should be noted that the FRZB_E186 CpG locus rather than FRZB_P406 was significantly differentially methylated in sample set #2. The AUC's for CpG sites within these genes remained high in sample set #2, ranging from 0.79 to 0.97. See Conway et al., 2011, Pigment Cell Melanoma Res. 24 352-360, and supplemental materials, the contents of which are hereby incorporated by reference.
  • Additional confirmation of the methylation specific markers is found in Table 8 below that shows 168 CpG sites that distinguish melanomas from benign nevi after Bonferroni correction.
  • TABLE 8
    Mole Mel
    Mean Mean Mean
    Target ID Raw_p Bonferron i_p FDR_p AUC β β Δβ
    ACTG2_P346F 4.42E−07 0.000434634 3.62E−06 0.780 0.921 0.819 0.101
    AFF3_P122_F 4.63E−13 4.56E−10 1.57E−11 0.883 0.963 0.882 0.080
    ALOX12_E85_R 2.83E−09 2.78E−06 3.98E−08 0.824 0.325 0.651 −0.327
    APBA2_P227_F 9.39E−07 0.000923948 7.22E−06 0.774 0.971 0.937 0.034
    APOA1_P261_F 8.02E−10 7.89E−07 1.27E−08 0.837 0.932 0.796 0.136
    AREG_P217_R 3.20E−05 0.031506185 0.000169388 0.734 0.184 0.130 0.054
    ATP10A_P524_R 3.43E−06 0.003377711 2.27E−05 0.778 0.814 0.633 0.182
    B3GALT5_P330_F 8.65E−10 8.51E−07 1.35E−08 0.833 0.957 0.867 0.090
    BCL3_E71_F 7.62E−06 0.007494111 4.54E−05 0.750 0.459 0.314 0.144
    BLK_P668_R 1.22E−18 1.20E−15 1.32E−16 0.944 0.963 0.834 0.129
    BMP4_P199_R 4.83E−05 0.047524599 0.000240023 0.731 0.622 0.753 −0.131
    BMPR1A_E88_F 2.00E−06 0.001968243 1.42E−05 0.765 0.817 0.627 0.190
    C4B_P191_F 9.65E−06 0.00949199 5.65E−05 0.748 0.975 0.951 0.024
    CARD15_P302_R 1.16E−09 1.15E−06 1.74E−08 0.833 0.489 0.211 0.278
    CASP8_E474_F 6.64E−06 0.006538478 4.01E−05 0.752 0.780 0.554 0.226
    CCL3_E53_R 1.00E−14 9.86E−12 4.33E−13 0.904 0.928 0.770 0.158
    CD1A_P414_R 5.58E−07 0.000548982 4.46E−06 0.778 0.949 0.878 0.071
    CD2_P68_F 1.78E−17 1.75E−14 1.17E−15 0.933 0.927 0.728 0.198
    CD34_P339_R 2.67E−06 0.002628299 1.82E−05 0.762 0.916 0.808 0.108
    CD34_P780_R 3.39E−08 3.34E−05 4.07E−07 0.804 0.837 0.653 0.184
    CD86_P3_F 1.67E−08 1.64E−05 2.13E−07 0.810 0.772 0.489 0.283
    COL1A1_P117_R 3.50E−11 3.44E−08 6.75E−10 0.856 0.694 0.359 0.335
    COL1A2_E299_F 1.93E−06 0.001897802 1.40E−05 0.765 0.066 0.280 −0.214
    COMT_E401_F 2.44E−07 0.000239712 2.24E−06 0.786 0.314 0.187 0.128
    CRK_P721_F 7.01E−06 0.006895396 4.20E−05 0.753 0.483 0.290 0.194
    CSF2_E248_R 5.55E−08 5.47E−05 6.28E−07 0.801 0.946 0.879 0.068
    CSF3_E242_R 2.98E−07 0.000292827 2.69E−06 0.784 0.959 0.904 0.055
    CSF3_P309_R 2.54E−07 0.000249538 2.31E−06 0.785 0.887 0.783 0.105
    DAB2IP_E18_R 4.04E−05 0.039721765 0.000206884 0.732 0.162 0.100 0.062
    DES_P1006_R 7.68E−08 7.55E−05 8.39E−07 0.796 0.905 0.801 0.105
    DLC1_P695_F 1.89E−12 1.86E−09 5.04E−11 0.875 0.941 0.804 0.137
    DMP1_P134_F 8.35E−08 8.22E−05 8.74E−07 0.796 0.912 0.821 0.091
    DSG1_E292_F 9.97E−09 9.81E−06 1.31E−07 0.816 0.897 0.742 0.154
    DSG1_P159_R 9.57E−10 9.42E−07 1.45E−08 0.832 0.697 0.398 0.299
    DSP_P36F 7.03E−07 0.000691676 5.53E−06 0.775 0.212 0.125 0.088
    EG F_P242_R 1.91E−16 1.88E−13 1.11E−14 0.923 0.955 0.864 0.091
    EMR3_E61_F 1.49E−18 1.46E−15 1.33E−16 0.943 0.880 0.524 0.355
    EMR3_P39_R 6.28E−16 6.18E−13 3.43E−14 0.919 0.862 0.567 0.295
    EPHB4_E476_R 2.07E−07 0.00020398 1.96E−06 0.787 0.333 0.209 0.124
    EPHB4_P313_R 4.14E−08 4.08E−05 4.86E−07 0.818 0.269 0.114 0.154
    EPHX1_P22_F 5.79E−06 0.005698994 3.56E−05 0.753 0.959 0.914 0.045
    EVI2A_E420_F 3.27E−18 3.22E−15 2.68E−16 0.940 0.964 0.851 0.113
    EVI2A_P94_R 9.81E−16 9.66E−13 5.08E−14 0.919 0.825 0.436 0.389
    FANCE_P356_R 3.10E−07 0.00030472 2.72E−06 0.783 0.397 0.207 0.190
    FASTK_P257_F 8.98E−07 0.000883867 7.01E−06 0.774 0.114 0.066 0.048
    FER_E119_F 3.81E−06 0.003753345 2.47E−05 0.759 0.210 0.122 0.087
    FGF12_E61_R 3.95E−06 0.003889874 2.54E−05 0.759 0.198 0.119 0.079
    FGF6_E294_F 1.03E−05 0.010164268 5.98E−05 0.756 0.941 0.838 0.103
    FGF6_P139_R 6.16E−06 0.006062049 3.74E−05 0.759 0.947 0.820 0.127
    FGFR1_E317_F 1.04E−11 1.02E−08 2.27E−10 0.864 0.118 0.065 0.053
    FLI1_E29_F 3.99E−06 0.003924016 2.55E−05 0.759 0.132 0.084 0.047
    FOSL2_E384_R 1.91E−07 0.000188082 1.83E−06 0.788 0.943 0.891 0.052
    FRZB_E186_R 3.43E−09 3.38E−06 4.69E−08 0.823 0.251 0.617 −0.366
    FRZB_P406_F 3.36E−07 0.000330741 2.84E−06 0.784 0.066 0.433 −0.367
    FZD9_P175_F 1.01E−12 9.91E−10 2.91E−11 0.878 0.212 0.123 0.089
    GABRA5_P1016_F 3.31E−12 3.26E−09 8.14E−11 0.871 0.945 0.812 0.133
    GML_P281_R 3.71E−06 0.003652683 2.42E−05 0.760 0.899 0.756 0.143
    GPR116_P850_F 2.92E−09 2.87E−06 4.04E−08 0.829 0.938 0.878 0.061
    HBII-52_P563_F 9.45E−13 9.30E−10 2.82E−11 0.879 0.890 0.624 0.266
    HBII-52_P659_F 1.15E−07 0.00011289 1.16E−06 0.799 0.953 0.859 0.095
    HGF_P1293_R 1.61E−06 0.001580085 1.20E−05 0.767 0.966 0.930 0.036
    HLA-DPA1_P28_R 2.59E−12 2.54E−09 6.69E−11 0.873 0.849 0.520 0.329
    HLA-DPB1_E2_R 2.70E−12 2.66E−09 6.82E−11 0.886 0.666 0.376 0.290
    HLA-DRA_P77_R 1.23E−06 0.00120708 9.29E−06 0.771 0.407 0.197 0.210
    HOXA9_E252_R 1.98E−06 0.001950492 1.42E−05 0.777 0.247 0.595 −0.349
    HPN_P374_R 1.42E−05 0.013956409 8.02E−05 0.755 0.525 0.669 −0.144
    HTR2A_E10_R 8.72E−06 0.008580868 5.17E−05 0.749 0.944 0.882 0.062
    IAPP_E280_F 3.02E−08 2.97E−05 3.72E−07 0.813 0.943 0.873 0.070
    IFNG_P459_R 7.75E−23 7.63E−20 2.54E−20 0.985 0.843 0.529 0.314
    IL12B_P1453_F 1.48E−05 0.014570463 8.33E−05 0.744 0.877 0.781 0.097
    IL13_E75_R 2.67E−06 0.002628299 1.82E−05 0.762 0.972 0.944 0.028
    IL1B_P582_R 4.49E−06 0.004415524 2.83E−05 0.759 0.918 0.813 0.105
    IL2_P607_R 3.19E−13 3.14E−10 1.12E−11 0.891 0.879 0.640 0.239
    INS_P248_F 3.00E−07 0.000295448 2.69E−06 0.789 0.853 0.655 0.198
    IPF1_P750_F 2.69E−06 0.002643505 1.82E−05 0.765 0.399 0.593 −0.194
    ITK_E166_R 1.35E−18 1.32E−15 1.32E−16 0.943 0.951 0.762 0.188
    ITK_P114_F 4.48E−20 4.41E−17 6.92E−18 0.956 0.898 0.636 0.262
    JAG1_P66_F 3.36E−07 0.000330741 2.84E−06 0.784 0.142 0.092 0.050
    KCNK4_E3_F 1.50E−07 0.000147184 1.49E−06 0.790 0.236 0.509 −0.273
    KIAA0125_E29_F 5.03E−05 0.049508182 0.000248693 0.732 0.868 0.733 0.135
    KLK10_P268_R 8.20E−08 8.07E−05 8.74E−07 0.797 0.669 0.399 0.270
    KLK11_P103_R 4.76E−06 0.004688393 2.95E−05 0.757 0.746 0.528 0.218
    KLK11_P1290_F 1.61E−07 0.000158742 1.59E−06 0.791 0.926 0.837 0.089
    KRT1_P798_R 2.94E−17 2.89E−14 1.81E−15 0.939 0.841 0.604 0.237
    LAT_E46_F 8.15E−13 8.02E−10 2.51E−11 0.889 0.885 0.601 0.285
    LCK_E28_F 1.01E−14 9.96E−12 4.33E−13 0.906 0.960 0.870 0.089
    LMO2_E148_F 2.42E−11 2.38E−08 4.86E−10 0.860 0.967 0.927 0.040
    LOX_P313_R 1.89E−05 0.018560597 0.000104862 0.742 0.115 0.380 −0.266
    LTA_P214_R 3.43E−11 3.38E−08 6.75E−10 0.858 0.944 0.833 0.111
    LTB4R_P163_F 3.50E−12 3.44E−09 8.40E−11 0.873 0.920 0.793 0.127
    MAF_E77_R 1.02E−05 0.010062142 5.95E−05 0.748 0.135 0.067 0.069
    MALT1_P406_R 3.23E−06 0.003180027 2.15E−05 0.763 0.148 0.076 0.071
    MAPK14_P327_R 4.71E−06 0.004635345 2.93E−05 0.760 0.177 0.088 0.089
    MATK_P190_R 5.05E−05 0.049738537 0.000248693 0.736 0.289 0.179 0.110
    MEST_P62_R 9.33E−06 0.009178578 5.50E−05 0.748 0.305 0.509 −0.204
    MMP10_E136_R 3.60E−09 3.54E−06 4.85E−08 0.822 0.894 0.707 0.187
    MMP19_E274_R 1.55E−06 0.001522929 1.16E−05 0.767 0.922 0.839 0.083
    MMP2_P197_F 4.08E−08 4.02E−05 4.84E−07 0.804 0.648 0.386 0.263
    MMP2_P303_R 5.05E−13 4.97E−10 1.66E−11 0.884 0.831 0.497 0.334
    MMP9_P237_R 1.99E−06 0.001959709 1.42E−05 0.768 0.200 0.106 0.094
    MOS_P746_F 1.76E−05 0.017361256 9.86E−05 0.743 0.789 0.611 0.178
    MPL_P62_F 9.37E−07 0.000921959 7.22E−06 0.784 0.938 0.887 0.051
    MPO_P883_R 1.72E−21 1.69E−18 3.38E−19 0.967 0.686 0.207 0.479
    MSH3_E3_F 1.55E−10 1.53E−07 2.63E−09 0.846 0.878 0.769 0.109
    MSH3_P13_R 2.41E−05 0.023709722 0.000130993 0.737 0.740 0.585 0.155
    MST1R_P87_R 3.68E−06 0.003620829 2.41E−05 0.758 0.446 0.629 −0.184
    MUSK_P308_F 3.37E−07 0.000331991 2.84E−06 0.784 0.917 0.790 0.127
    NDN_P1110_F 3.12E−07 0.000307373 2.72E−06 0.787 0.922 0.814 0.108
    NEFL_E23_R 1.83E−09 1.80E−06 2.68E−08 0.828 0.267 0.509 −0.242
    NEU1_P745_F 4.61E−07 0.00045392 3.75E−06 0.782 0.217 0.097 0.120
    NOS2A_E117_R 1.95E−13 1.92E−10 7.12E−12 0.888 0.954 0.891 0.064
    NOTCH4_P938_F 3.76E−15 3.70E−12 1.76E−13 0.909 0.929 0.790 0.139
    NPR2_P1093_F 2.36E−05 0.023191257 0.00012956 0.740 0.680 0.787 −0.107
    OPCML_P71_F 5.89E−13 5.79E−10 1.87E−11 0.885 0.747 0.332 0.415
    OSM_P188_F 1.23E−17 1.21E−14 8.66E−16 0.935 0.956 0.794 0.162
    OSM_P34_F 6.92E−10 6.81E−07 1.12E−08 0.842 0.915 0.737 0.178
    PADI4_E24_F 8.01E−08 7.88E−05 8.66E−07 0.796 0.854 0.651 0.203
    PDGFA_P78_F 5.99E−06 0.005898733 3.66E−05 0.753 0.242 0.153 0.088
    PDGFRA_E125_F 4.52E−08 4.44E−05 5.23E−07 0.804 0.869 0.660 0.209
    PECAM1_P135_F 6.81E−11 6.70E−08 1.24E−09 0.853 0.916 0.777 0.139
    PEG3_E496_F 3.72E−05 0.03657662 0.000191501 0.735 0.658 0.487 0.171
    PGR_E183_R 2.78E−10 2.74E−07 4.64E−09 0.842 0.860 0.643 0.217
    PI3_P1394_R 1.01E−07 9.95E−05 1.04E−06 0.802 0.575 0.318 0.257
    PLA2G2A_E268_F 1.15E−08 1.13E−05 1.48E−07 0.814 0.867 0.689 0.178
    PLG_E406_F 2.24E−14 2.21E−11 8.83E−13 0.900 0.962 0.887 0.075
    PMP22_P975_F 4.60E−06 0.004525044 2.88E−05 0.757 0.936 0.849 0.087
    PROM1_P44_R 5.52E−07 0.000542987 4.45E−06 0.781 0.945 0.891 0.054
    PRSS1_E45_R 2.25E−07 0.000221013 2.10E−06 0.788 0.768 0.541 0.227
    PRSS1_P1249_R 3.47E−05 0.034151828 0.000181659 0.740 0.658 0.463 0.196
    PSCA_E359_F 3.41E−05 0.033539227 0.000179354 0.733 0.835 0.678 0.157
    PTHLH_E251_F 3.95E−19 3.88E−16 4.85E−17 0.948 0.883 0.669 0.214
    PTHLH_P757_F 1.07E−10 1.05E−07 1.91E−09 0.850 0.930 0.848 0.083
    PTHR1_P258_F 2.31E−06 0.002277735 1.63E−05 0.765 0.781 0.583 0.198
    PTK6_E50_F 4.22E−05 0.041567996 0.000214786 0.733 0.719 0.489 0.230
    PTK7_E317_F 1.13E−10 1.11E−07 1.98E−09 0.850 0.609 0.361 0.248
    PWCR1_E81_R 3.96E−18 3.90E−15 3.00E−16 0.939 0.974 0.884 0.090
    PWCR1_P357_F 8.35E−08 8.22E−05 8.74E−07 0.796 0.865 0.700 0.165
    PXN_P308_F 1.22E−05 0.011986257 6.97E−05 0.745 0.331 0.205 0.126
    RARA_E128_R 1.86E−06 0.001829761 1.36E−05 0.766 0.102 0.296 −0.195
    RARA_P176_R 1.02E−06 0.00100545 7.79E−06 0.776 0.368 0.590 −0.222
    RARRES1_P57_R 4.87E−08 4.79E−05 5.57E−07 0.802 0.724 0.491 0.233
    RIPK3_P124_F 3.30E−07 0.000324591 2.84E−06 0.787 0.382 0.650 −0.267
    RUNX3_E27_R 1.17E−21 1.15E−18 2.87E−19 0.967 0.935 0.622 0.313
    RUNX3_P247_F 4.92E−20 4.84E−17 6.92E−18 0.957 0.955 0.666 0.289
    RUNX3_P393_R 4.05E−24 3.99E−21 2.37E−21 0.981 0.946 0.705 0.241
    S100A2_P1186_F 4.37E−05 0.042970545 0.000220362 0.730 0.744 0.541 0.202
    S100A4_P194_R 1.75E−07 0.000172513 1.71E−06 0.790 0.871 0.698 0.173
    SEMA3B_E96_F 1.44E−07 0.000141254 1.44E−06 0.791 0.643 0.387 0.255
    SEMA3B_P110_R 2.26E−05 0.022243687 0.000124965 0.738 0.687 0.439 0.248
    SERPINA5_E69_F 6.65E−09 6.55E−06 8.85E−08 0.817 0.839 0.651 0.188
    SERPINA5_P156_F 1.66E−06 0.0016315 1.23E−05 0.768 0.547 0.345 0.201
    SERPIN B2_P939_F 3.00E−06 0.002955566 2.02E−05 0.790 0.954 0.917 0.037
    SFN_P248_F 1.22E−05 0.011986257 6.97E−05 0.745 0.351 0.215 0.136
    SFTPA1_P421_F 1.93E−11 1.90E−08 4.04E−10 0.868 0.928 0.823 0.106
    SFTPB_P689_R 2.41E−06 0.002375967 1.69E−05 0.778 0.889 0.821 0.068
    SFTPD_E169_F 1.47E−12 1.45E−09 4.03E−11 0.876 0.934 0.809 0.125
    SHB_P691_R 4.09E−06 0.004024225 2.60E−05 0.757 0.634 0.376 0.258
    SIN3B_P514_R 1.80E−07 0.000177418 1.74E−06 0.793 0.924 0.815 0.109
    SLC14A1_E295_F 1.39E−13 1.37E−10 5.27E−12 0.890 0.904 0.719 0.185
    SLC22A2_E271_R 3.11E−07 0.000306227 2.72E−06 0.785 0.967 0.897 0.070
    SLC22A3_P634_F 4.23E−05 0.041668393 0.000214786 0.730 0.820 0.668 0.152
    SNRPN_E14_F 3.56E−05 0.035015362 0.000185266 0.734 0.880 0.734 0.146
    SNRPN_P230_R 9.73E−08 9.57E−05 1.01E−06 0.796 0.941 0.844 0.097
    SNRPN_seq_18_S99_F 1.98E−08 1.95E−05 2.50E−07 0.813 0.824 0.645 0.178
    SNURF_P2_R 6.48E−08 6.37E−05 7.16E−07 0.798 0.671 0.473 0.198
    SNURF_P78_F 4.64E−05 0.045690286 0.000233114 0.729 0.815 0.642 0.173
    SPI1_1348_F 4.49E−12 4.42E−09 1.05E−10 0.869 0.961 0.856 0.105
    STAT5A_E42_F 4.08E−07 0.000401853 3.38E−06 0.781 0.356 0.212 0.144
    SYK_P584_F 4.00E−11 3.94E−08 7.57E−10 0.859 0.893 0.708 0.185
    TDG_E129_F 5.72E−12 5.63E−09 1.31E−10 0.868 0.835 0.665 0.170
    TEK_P526_F 3.11E−08 3.06E−05 3.77E−07 0.804 0.846 0.716 0.131
    TFF2_P557_R 2.57E−09 2.53E−06 3.66E−08 0.825 0.967 0.923 0.043
    TGFB3_E58_R 6.48E−08 6.37E−05 7.16E−07 0.798 0.845 0.891 −0.046
    THPO_E483_F 2.34E−07 0.000230256 2.17E−06 0.786 0.967 0.923 0.043
    TIE1_E66_R 4.83E−10 4.76E−07 7.93E−09 0.839 0.938 0.833 0.106
    TJP2_P518_F 1.12E−11 1.10E−08 2.40E−10 0.865 0.346 0.149 0.197
    TMEM63A_E63_F 2.88E−05 0.028340214 0.000154023 0.739 0.138 0.052 0.086
    TNFRSF10D_E27_F 1.24E−05 0.012194527 7.05E−05 0.746 0.401 0.596 −0.195
    TNFSF10_E53_F 2.49E−08 2.45E−05 3.10E−07 0.806 0.552 0.275 0.277
    TNFSF10_P2_R 2.38E−05 0.023396482 0.00012998 0.744 0.839 0.612 0.227
    TNFSF8_E258_R 4.81E−24 4.74E−21 2.37E−21 0.981 0.929 0.593 0.336
    TNFSF8_P184_F 2.21E−11 2.18E−08 4.54E−10 0.859 0.565 0.255 0.311
    TRAF4_P372_F 1.55E−10 1.53E−07 2.63E−09 0.846 0.313 0.163 0.150
    TRIP6_P1090_F 2.01E−09 1.98E−06 2.91E−08 0.827 0.357 0.688 −0.332
    TRIP6_P1274_R 2.82E−05 0.027782809 0.000151819 0.735 0.451 0.655 −0.203
    TRPM5_E87_F 1.45E−14 1.43E−11 5.94E−13 0.902 0.935 0.794 0.140
    TSG101_P257_R 8.97E−10 8.83E−07 1.38E−08 0.846 0.400 0.188 0.212
    TWIST1_P44_R 3.61E−05 0.035511764 0.000186904 0.739 0.158 0.072 0.086
    UGT1A1_E11_F 6.07E−12 5.98E−09 1.36E−10 0.867 0.971 0.922 0.049
    UGT1A1_P315_R 4.08E−11 4.01E−08 7.57E−10 0.857 0.875 0.706 0.169
    UGT1A1_P564_R 3.20E−05 0.031506185 0.000169388 0.734 0.967 0.920 0.047
    USP29_P282_R 3.81E−07 0.000374549 3.17E−06 0.783 0.948 0.889 0.059
    VAV1_E9_F 5.80E−07 0.000570634 4.60E−06 0.777 0.420 0.229 0.191
    WNT10B_P993_F 4.79E−05 0.047109973 0.000239137 0.729 0.270 0.189 0.081
    WNT8B_E487_F 1.27E−15 1.25E−12 6.25E−14 0.926 0.897 0.769 0.128
    WNT8B_P216_R 1.41E−12 1.39E−09 3.96E−11 0.893 0.952 0.922 0.030
    WRN_P969_F 3.19E−06 0.00314233 2.14E−05 0.760 0.932 0.849 0.084
    ZIM3_E203_F 1.73E−06 0.001700572 1.27E−05 0.766 0.971 0.927 0.044
    ZNFN1A1_E102_F 2.69E−06 0.002643505 1.82E−05 0.765 0.855 0.715 0.140
    ZNFN1A1_P179_F 2.60E−05 0.025596467 0.00014064 0.739 0.969 0.943 0.026
    • 6.11. Comparison of Methylation Profiles in Benign and Dysplastic Nevi, Primary Malignant Melanomas and Metastatic Melanoma
  • Illumina GoldenGate Cancer Panel I methylation profiling was performed in metastatic melanomas (n=11) to evaluate promoter methylation patterns. Illumina methylation array results were subjected to filtering using the same criterion as in the earlier sets of nevi and melanoma. Using class comparison analyses, promoter methylation patterns of metastatic melanomas were compared to promoter methylation patterns in benign and dysplastic nevi (n=56), and primary melanomas (n=47). Initial results found 91 CpG sites hypermethylated and 72 CpG sites hypomethylated in metastases when compared to nevi. (Table 5A/B) After Bonferroni correction for multiple comparisons, 75 CpG sites were identified that differed significantly (with P values of ≦0.05) between nevi and metastatic melanomas. Comparison of statistically significant sites of nevi and melanoma to nevi and metastases identified 31 overlapping CpG sites. No statistically significant differences in methylation patterns were seen between primary melanomas and metastatic melanomas for the CpG sites identified to define nevi.
  • FIG. 5 shows a Venn diagram of CpG sites that statistically significantly distinguish between nevi (dysplastic and non-dysplastic) and primary melanomas or metastases. The number of statistically significant differential CpG sites, after Bonferoni correction for multiple comparisons and adjusting for age and gender, (p≦0.05) are listed for each of the three comparisons. The diagram is based on sample sets of nevi (n=56), melanoma (n=47), and metastases (n=11). 58 CpG sites distinguish between nevi and melanomas. 75 CpG sites distinguish between nevi and metastases. 31 common CpG sites differentiate nevi from either primary melanomas or metastases.
    • 6.12. Methylation Markers for Normal Skin
  • Because normal skin may be a confounding contaminant for mole or melanoma samples, an analysis was undertaken to find methylation markers for normal skin. Using the methods described above, profiling was performed on FFPE normal skin specimens (N=42) discarded from surgeries. Tables 9A-9D below show the results of this analysis.
  • TABLE 9A
    Statistically significant CpGs between skin and melanoma
    p. val. skin. q. val. skin. coef. skin. mean. mean. mean.
    ProbeID v. mela v. mela v. mela β. skin β. mela β. diff
    AATK_E63_R 1.04E−07 1.52E−06 1.4214 0.695 0.904 −0.209
    AATK_P519_R 5.77E−11 2.54E−09 1.8072 0.609 0.904 −0.295
    AATK_P709_R 8.09E−09 1.64E−07 1.9841 0.288 0.730 −0.442
    ALOX12_P223_R 3.72E−11 1.80E−09 2.4206 0.211 0.740 −0.528
    AXL_P223_R 9.49E−08 1.40E−06 1.7792 0.079 0.336 −0.258
    BMP4_P199_R 3.37E−11 1.69E−09 2.0563 0.395 0.831 −0.435
    CALCA_P171_F 0.000318 0.001586 0.9918 0.254 0.477 −0.223
    CAPG_E228_F 4.94E−06 4.44E−05 1.5022 0.196 0.512 −0.316
    CASP10_P334_F 0.000221 0.001143 1.1924 0.200 0.450 −0.250
    CDH13_P88_F 2.11E−07 2.72E−06 1.8729 0.183 0.593 −0.410
    COL1A2_P407_R 5.62E−08 8.79E−07 1.7663 0.326 0.736 −0.411
    CPA4_E20_F 0.000484 0.002202 1.0139 0.263 0.494 −0.231
    CRIP1_P274_F 3.29E−05 0.000227 1.3256 0.309 0.627 −0.317
    CRIP1_P874_R 2.78E−13 5.07E−11 2.2923 0.082 0.465 −0.383
    CSF1R_P73_F 4.76E−07 5.13E−06 1.3677 0.328 0.653 −0.325
    CSF3R_P8_F 0.003225 0.011268 0.9969 0.439 0.677 −0.238
    DDR1_P332_R 8.60E−12 6.26E−10 2.4730 0.289 0.827 −0.538
    EYA4_P794_F 0.001818 0.006894 1.1556 0.359 0.640 −0.281
    FGF9_P862_R 7.43E−13 9.01E−11 1.2886 0.145 0.380 −0.235
    GJB2_P931_R 5.18E−08 8.20E−07 1.6722 0.376 0.762 −0.386
    GRB10_P496_R 3.76E−05 0.000257 1.4099 0.479 0.786 −0.306
    GRB7_E71_R 5.51E−14 1.61E−11 2.1378 0.129 0.553 −0.424
    GRB7_P160_R 4.87E−07 5.15E−06 1.6047 0.415 0.778 −0.363
    HCK_P858_F 0.000134 0.000757 1.4883 0.379 0.715 −0.335
    HOXA9_P303_F 6.25E−09 1.34E−07 2.0299 0.073 0.375 −0.302
    IFNGR2_P377_R 0.000347 0.001693 1.3107 0.247 0.548 −0.301
    IGFBP1_E48_R 8.48E−10 2.42E−08 1.9080 0.651 0.926 −0.275
    IGFBP1_P12_R 0.000135 0.000757 1.1764 0.645 0.853 −0.208
    IL17RB_P788_R 7.21E−10 2.19E−08 2.5332 0.062 0.451 −0.389
    IL1RN_E42_F 3.57E−07 3.99E−06 1.1514 0.625 0.840 −0.215
    IL1RN_P93_R 2.36E−10 7.99E−09 1.6854 0.379 0.765 −0.386
    IPF1_P234_F 0.000275 0.001387 1.2457 0.312 0.604 −0.293
    JAK3_P1075_R 2.78E−09 6.64E−08 1.6399 0.449 0.806 −0.358
    KIAA1804_P689_R 7.39E−08 1.13E−06 2.2881 0.068 0.415 −0.347
    LEFTY2_P561_F 0.00011 0.000644 1.0741 0.384 0.644 −0.260
    LY6G6E_P45_R 2.24E−10 7.78E−09 1.7792 0.599 0.898 −0.299
    MEST_E150_F 4.74E−05 0.000308 1.2153 0.310 0.598 −0.288
    MET_E333_F 7.83E−06 6.63E−05 1.4735 0.220 0.545 −0.325
    MMP7_E59_F 7.68E−06 6.54E−05 1.1203 0.286 0.550 −0.264
    MPO_P883_R 0.00041 0.00192 −1.0215 0.425 0.211 0.215
    MST1R_E42_R 1.97E−10 6.99E−09 2.1092 0.264 0.743 −0.479
    MUC1_E18_R 1.55E−10 6.10E−09 1.5059 0.553 0.847 −0.294
    NBL1_E205_R 6.49E−07 6.66E−06 1.4316 0.524 0.819 −0.295
    NBL1_P24_F 8.63E−07 8.78E−06 1.5593 0.309 0.680 −0.371
    PDGFRA_E125_F 0.000207 0.001086 1.2002 0.489 0.759 −0.270
    PLAU_P176_R 7.39E−10 2.20E−08 2.2742 0.070 0.418 −0.348
    POMC_P400_R 2.31E−07 2.89E−06 1.8722 0.280 0.715 −0.435
    PRSS8_E134_R 2.13E−13 4.42E−11 1.9091 0.664 0.930 −0.266
    PTPN6_E171_R 3.81E−07 4.24E−06 1.8056 0.314 0.727 −0.413
    PTPRO_P371_F 0.000309 0.001544 1.2753 0.154 0.394 −0.239
    RARA_P176_R 1.53E−07 2.06E−06 1.9454 0.237 0.681 −0.444
    SEMA3A_P343_F 3.62E−05 0.000248 1.4898 0.118 0.365 −0.247
    SEMA3B_P110_R 1.59E−05 0.00012 1.3407 0.121 0.343 −0.222
    SERPINE1_E189_R 4.00E−07 4.41E−06 1.5515 0.179 0.500 −0.321
    SHB_P691_R 9.72E−07 9.76E−06 1.7027 0.097 0.366 −0.270
    SNCG_E119_F 3.29E−11 1.69E−09 2.1366 0.260 0.748 −0.487
    SNCG_P53_F 1.02E−08 2.02E−07 2.1023 0.286 0.761 −0.476
    SNCG_P98_R 0.00054 0.002414 0.8917 0.481 0.692 −0.211
    SPDEF_P6_R 1.39E−09 3.67E−08 1.8819 0.362 0.784 −0.423
    SPP1_E140_R 0.000433 0.001999 1.0557 0.412 0.666 −0.254
    STAT5A_P704_R 6.56E−08 1.02E−06 1.8785 0.199 0.618 −0.419
    TAL1_P594_F 2.35E−05 0.00017 1.4210 0.383 0.713 −0.330
    TEK_E75_F 0.000186 0.000996 1.1881 0.528 0.785 −0.257
    TGFB2_E226_R 1.81E−17 8.81E−15 3.3352 0.150 0.831 −0.681
    TGFB3_E58_R 6.03E−11 2.58E−09 1.8890 0.571 0.898 −0.327
    TGFBI_P173_F 0.000122 0.00071 1.4164 0.116 0.346 −0.230
    THBS2_P605_R 3.27E−05 0.000227 1.6874 0.237 0.624 −0.387
    THY1_P149_R 7.03E−05 0.000432 1.2327 0.149 0.374 −0.225
    TNFRSF10A_P171_F 2.45E−07 3.00E−06 1.9202 0.155 0.547 −0.392
    TNFRSF10D_E27_F 6.47E−18 4.71E−15 3.1605 0.125 0.752 −0.627
    TNFRSF10D_P70_F 5.96E−13 8.68E−11 2.2537 0.193 0.678 −0.485
    TNFSF10_E53_F 1.37E−07 1.88E−06 1.7039 0.108 0.395 −0.288
    TNFSF10_P2_R 9.69E−11 3.92E−09 2.8088 0.150 0.742 −0.591
    WNT10B_P823_R 0.003172 0.011235 1.1306 0.309 0.574 −0.265
  • TABLE 9B
    Statistically significant CpGs between skin and moles
    p. val. skin. q. val. skin. coef. skin. mean. beta. mean. beta. mean. beta.
    ProbeID v. mole v. mole v. mole skin mole diff
    AATK_E63_R 2.17E−08 3.44E−07 1.3860 0.700 0.903 −0.202
    AATK_P519_R 9.76E−09 1.69E−07 1.5241 0.631 0.886 −0.255
    AATK_P709_R 9.26E−08 1.20E−06 1.6614 0.300 0.690 −0.390
    ALOX12_P223_R 5.53E−06 3.80E−05 1.4178 0.183 0.475 −0.292
    AXL_P223_R 9.20E−09 1.61E−07 1.7461 0.070 0.299 −0.229
    BMP4_P199_R 3.90E−06 2.91E−05 1.4192 0.364 0.695 −0.331
    CALCA_P171_F 0.000664 0.00212 0.9302 0.239 0.442 −0.203
    CAPG_E228_F 5.33E−12 2.50E−10 2.3537 0.186 0.706 −0.520
    CASP10_P334_F 2.38E−12 1.24E−10 1.8892 0.171 0.566 −0.395
    CDH13_P88_F 5.60E−05 0.000259 1.1776 0.177 0.411 −0.234
    COL1A2_P407_R 2.09E−11 7.80E−10 2.0681 0.329 0.795 −0.466
    CPA4_E20_F 5.07E−06 3.56E−05 1.2938 0.261 0.563 −0.302
    CRIP1_P274_F 1.44E−09 3.32E−08 1.8763 0.283 0.715 −0.432
    CRIP1_P874_R 1.98E−21 4.80E−19 2.6804 0.080 0.560 −0.479
    CSF1R_P73_F 2.08E−07 2.34E−06 1.3586 0.342 0.667 −0.325
    CSF3R_P8_F 7.06E−10 1.71E−08 2.0001 0.458 0.859 −0.401
    DDR1_P332_R 9.70E−10 2.32E−08 2.0063 0.263 0.721 −0.459
    EYA4_P794_F 0.017419 0.03324 0.8850 0.361 0.578 −0.217
    FGF9_P862_R 2.07E−13 1.37E−11 1.4261 0.137 0.397 −0.260
    GJB2_P931_R 1.48E−07 1.84E−06 1.6227 0.381 0.757 −0.376
    GRB10_P496_R 5.69E−06 3.87E−05 1.3395 0.471 0.772 −0.301
    GRB7_E71_R 5.71E−10 1.44E−08 1.8195 0.107 0.404 −0.297
    GRB7_P160_R 2.68E−10 7.23E−09 1.8566 0.392 0.803 −0.411
    HCK_P858_F 0.000129 0.00052 1.2238 0.346 0.637 −0.291
    HOXA9_P303_F 8.84E−09 1.58E−07 1.7524 0.067 0.293 −0.226
    IFNGR2_P377_R 6.99E−07 6.65E−06 1.7076 0.249 0.646 −0.397
    IGFBP1_E48_R 4.44E−09 8.97E−08 1.9125 0.679 0.934 −0.255
    IGFBP1_P12_R 1.46E−06 1.22E−05 1.4924 0.645 0.890 −0.245
    IL17RB_P788_R 3.67E−20 7.63E−18 3.3227 0.055 0.612 −0.557
    IL1RN_E42_F 6.32E−07 6.13E−06 1.1331 0.630 0.841 −0.211
    IL1RN_P93_R 8.25E−12 3.53E−10 1.7523 0.375 0.776 −0.401
    IPF1_P234_F 0.000167 0.000645 1.1957 0.278 0.556 −0.278
    JAK3_P1075_R 1.54E−10 4.58E−09 1.7489 0.466 0.832 −0.366
    KIAA1804_P689_R 1.43E−10 4.33E−09 1.8411 0.065 0.305 −0.240
    LEFTY2_P561_F 2.55E−07 2.81E−06 1.2830 0.406 0.710 −0.304
    LY6G6E_P45_R 6.01E−08 8.31E−07 1.3572 0.603 0.855 −0.252
    MEST_E150_F 6.78E−05 0.000302 1.1353 0.264 0.512 −0.248
    MET_E333_F 6.15E−12 2.80E−10 1.9534 0.212 0.655 −0.443
    MMP7_E59_F 3.67E−12 1.84E−10 1.5096 0.281 0.637 −0.356
    MPO_P883_R 8.32E−11 2.69E−09 1.3782 0.435 0.753 −0.318
    MST1R_E42_R 6.05E−08 8.31E−07 1.6534 0.243 0.624 −0.381
    MUC1_E18_R 3.57E−09 7.52E−08 1.1762 0.551 0.799 −0.248
    NBL1_E205_R 1.24E−08 2.12E−07 1.3912 0.556 0.832 −0.276
    NBL1_P24_F 4.90E−09 9.64E−08 1.4422 0.308 0.653 −0.345
    PDGFRA_E125_F 3.53E−13 2.19E−11 2.2452 0.499 0.903 −0.404
    PLAU_P176_R 1.04E−14 8.44E−13 2.4790 0.063 0.445 −0.381
    POMC_P400_R 1.58E−11 6.23E−10 2.1786 0.316 0.797 −0.481
    PRSS8_E134_R 4.59E−12 2.23E−10 1.8324 0.645 0.918 −0.273
    PTPN6_E171_R 9.03E−20 1.64E−17 2.8980 0.298 0.885 −0.586
    PTPRO_P371_F 1.20E−05 7.21E−05 1.3796 0.141 0.386 −0.245
    RARA_P176_R 0.001157 0.003366 1.1595 0.197 0.429 −0.232
    SEMA3A_P343_F 2.33E−06 1.85E−05 1.4008 0.103 0.311 −0.207
    SEMA3B_P110_R 3.67E−19 5.34E−17 2.6197 0.120 0.651 −0.531
    SERPINE1_E189_R 1.00E−14 8.44E−13 2.1014 0.164 0.611 −0.447
    SHB_P691_R 1.42E−18 1.88E−16 3.0713 0.099 0.695 −0.596
    SNCG_E119_F 7.68E−11 2.54E−09 2.0937 0.274 0.752 −0.478
    SNCG_P53_F 2.41E−15 2.51E−13 2.8608 0.299 0.881 −0.582
    SNCG_P98_R 6.08E−06 4.10E−05 1.1626 0.528 0.777 −0.249
    SPDEF_P6_R 5.50E−15 5.34E−13 2.3115 0.365 0.851 −0.486
    SPP1_E140_R 2.15E−10 5.90E−09 1.8149 0.433 0.822 −0.388
    STAT5A_P704_R 7.14E−06 4.72E−05 1.3639 0.205 0.502 −0.297
    TAL1_P594_F 0.001295 0.00369 1.1308 0.338 0.606 −0.268
    TEK_E75_F 0.001369 0.003848 1.0130 0.525 0.753 −0.228
    TGFB2_E226_R 0.00013 0.00052 1.4123 0.145 0.407 −0.263
    TGFB3_E58_R 7.06E−07 6.68E−06 1.3078 0.565 0.828 −0.263
    TGFBI_P173_F 1.97E−06 1.59E−05 1.4111 0.101 0.313 −0.211
    THBS2_P605_R 7.83E−15 7.13E−13 3.1447 0.248 0.883 −0.635
    THY1_P149_R 1.98E−07 2.28E−06 1.3813 0.135 0.378 −0.244
    TNFRSF10A_P171_F 5.34E−07 5.32E−06 1.7166 0.129 0.442 −0.313
    TNFRSF10D_E27_F 3.11E−11 1.13E−09 2.1540 0.103 0.489 −0.386
    TNFRSF10D_P70_F 1.89E−22 1.37E−19 2.6349 0.172 0.740 −0.568
    TNFSF10_E53_F 7.09E−26 1.03E−22 3.2196 0.095 0.718 −0.622
    TNFSF10_P2_R 9.29E−22 3.38E−19 3.6021 0.174 0.879 −0.706
    WNT10B_P823_R 8.10E−07 7.42E−06 1.7577 0.301 0.710 −0.409
  • TABLE 9C
    Statistically significant CpGs between skin and moles and melanoma
    p. value. skin. q. value. skin. coef. skin. mean. mean. mean.
    ProbeID vs. mole vs. mole vs. mole beta. skin beta. mole beta. diff
    CAPG_E228_F 5.33E−12 2.50E−10 2.3537 0.186 0.706 −0.520
    MPO_P883_R 8.32E−11 2.69E−09 1.3782 0.435 0.753 −0.318
    RARA_P176_R 0.001157 0.003366 1.1595 0.197 0.429 −0.232
    SEMA3B_P110_R 3.67E−19 5.34E−17 2.6197 0.120 0.651 −0.531
    SHB_P691_R 1.42E−18 1.88E−16 3.0713 0.099 0.695 −0.596
    TGFB2_E226_R 0.00013 0.00052 1.4123 0.145 0.407 −0.263
    THBS2_P605_R 7.83E−15 7.13E−13 3.1447 0.248 0.883 −0.635
    TNFRSF10D_E27_F 3.11E−11 1.13E−09 2.1540 0.103 0.489 −0.386
    TNFSF10_E53_F 7.09E−26 1.03E−22 3.2196 0.095 0.718 −0.622
    WNT10B_P823_R 8.10E−07 7.42E−06 1.7577 0.301 0.710 −0.409

    Table 9D shows the accession numbers; specific single CpG coordinate; presence or absence of CpG islands; specific sequences used in the Illumina GoldenGate array experiments; and the synonyms for genes hypermethylated or hypomethylated in normal skin v. mole and melanoma analysis. All gene IDs and accession numbers are from Ref. Seq. version 36.1.
  • Probe_ID Gid Accession Gene_ID Chrm CpG_Coor Dist_to_TSS CpG_i
    AATK_E63_R 89041906 XM_927215.1 9625 17 76709831 63 N
    AATK_P519_R 89041906 XM_927215.1 9625 17 76710413 −519 Y
    AATK_P709_R 89041906 XM_927215.1 9625 17 76710603 −709 Y
    ALOX12_E85_R 4502050 NM_000697.1 239 17 6840213 85 Y
    ALOX12_P223_R 4502050 NM_000697.1 239 17 6839905 −223 Y
    ASCL2_P360_F 42716308 NM_005170.2 430 11 2249118 −360 Y
    ASCL2_P609_R 42716308 NM_005170.2 430 11 2249367 −609 Y
    AXL_P223_R 21536465 NM_021913.2 558 19 46416440 −223 Y
    B3GALT5_E246_R 15451880 NM_033170.1 10317 21 39951370 246 N
    BGN_P333_R 34304351 NM_001711.3 633 X 152413272 −333 N
    BLK_P14_F 33469981 NM_001715.2 640 8 11388916 −14 N
    BMP4_P123_R 19528651 NM_130851.1 652 14 53493485 −123 Y
    BMP4_P199_R 19528651 NM_130851.1 652 14 53493561 −199 Y
    CALCA_P171_F 76880483 NM_001033952.1 796 11 14950579 −171 Y
    CAPG_E228_F 63252912 NM_001747.2 822 2 85490959 228 N
    CASP10_E139_F 47078266 NM_001230.3 843 2 201756239 139 N
    CASP10_P334_F 47078266 NM_001230.3 843 2 201755766 −334 N
    CDH11_E102_R 16306531 NM_001797.2 1009 16 63713318 102 Y
    CDH11_P354_R 16306531 NM_001797.2 1009 16 63713774 −354 Y
    CDH13_P88_F 61676095 NM_001257.3 1012 16 81217991 −88 Y
    CFTR_P372_R 6995995 NM_000492.2 1080 7 116906881 −372 Y
    COL1A2_E299_F 48762933 NM_000089.3 1278 7 93862108 299 Y
    COL1A2_P407_R 48762933 NM_000089.3 1278 7 93861402 −407 N
    COL1A2_P48_R 48762933 NM_000089.3 1278 7 93861761 −48 Y
    CPA4_E20_F 61743915 NM_016352.2 51200 7 129720250 20 N
    CRIP1_P274_F 39725694 NM_001311.3 1396 14 105024320 −274 Y
    CRIP1_P874_R 39725694 NM_001311.3 1396 14 105023720 −874 Y
    CSF1R_P73_F 27262658 NM_005211.2 1436 5 149473201 −73 N
    CSF3R_P8_F 27437044 NM_172313.1 1441 1 36721104 −8 N
    CYP1B1_E83_R 13325059 NM_000104.2 1545 2 38156713 83 Y
    DDR1_P332_R 38327631 NM_001954.3 780 6 30959508 −332 N
    DDR2_E331_F 62420885 NM_001014796.1 4921 1 160869183 331 N
    DDR2_P743_R 62420885 NM_001014796.1 4921 1 160868109 −743 N
    DSC2_E90_F 40806177 NM_024422.2 1824 18 26936285 90 Y
    ELK3_P514_F 44955920 NM_005230.2 2004 12 95111824 −514 Y
    ELL_P693_F 47078265 NM_006532.2 8178 19 18494611 −693 Y
    EMR3_E61_F 23397638 NM_152939.1 84658 19 14646749 61 N
    EVI2A_P94_R 51511748 NM_001003927.1 2123 17 26672937 −94 N
    EYA4_P794_F 26667248 NM_004100.2 2070 6 133603412 −794 Y
    FANCE_P356_R 66879667 NM_021922.2 2178 6 35527760 −356 Y
    FGF9_P862_R 4503706 NM_002010.1 2254 13 21143013 −862 Y
    FGFR1_P204_F 13186232 NM_000604.2 2260 8 38445497 −204 Y
    FLT1_P615_R 32306519 NM_002019.2 2321 13 27967847 −615 Y
    FRZB_E186_R 38455387 NM_001463.2 2487 2 183439557 186 Y
    FRZB_P406_F 38455387 NM_001463.2 2487 2 183440149 −406 Y
    GFI1_P208_R 71037376 NM_005263.2 2672 1 92725229 −208 Y
    GJB2_P791_R 42558282 NM_004004.3 2706 13 19665828 −791 Y
    GJB2_P931_R 42558282 NM_004004.3 2706 13 19665968 −931 Y
    GNMT_P197_F 54792737 NM_018960.4 27232 6 43036281 −197 Y
    GP1BB_P278_R 9945387 NM_000407.3 2812 22 18090788 −278 Y
    GRB10_P496_R 48762696 NM_001001555.1 2887 7 50829148 −496 Y
    GRB7_E71_R 71979666 NM_001030002.1 2886 17 35147784 71 N
    GRB7_P160_R 71979666 NM_001030002.1 2886 17 35147553 −160 N
    GRPR_P200_R 61677286 NM_005314.2 2925 X 16051145 −200 N
    HBII-52_E142_F 29171307 NR_001291.1 338433 15 22967111 142 N
    HBII-52_P563_F 29171307 NR_001291.1 338433 15 22966406 −563 Y
    HCK_P858_F 30795228 NM_002110.2 3055 20 30102860 −858 Y
    HDAC7A_P344_F 13259521 NM_015401.1 51564 12 46479534 −344 N
    HFE_E273_R 21040354 NM_139010.1 3077 6 26195700 273 Y
    HHIP_P578_R 20143972 NM_022475.1 64399 4 145786045 −578 Y
    HOXA11_E35_F 24497552 NM_005523.4 3207 7 27191320 35 Y
    HOXA11_P92_R 24497552 NM_005523.4 3207 7 27191447 −92 Y
    HOXA9_E252_R 24497558 NM_002142.3 3205 7 27171422 252 Y
    HOXA9_P1141_R 24497558 NM_002142.3 3205 7 27172815 −1141 Y
    HOXA9_P303_F 24497558 NM_002142.3 3205 7 27171977 −303 Y
    HTR2A_P853_F 60302916 NM_000621.2 3356 13 46369029 −853 N
    IFNG_E293_F 56786137 NM_000619.2 3458 12 66839495 293 N
    IFNGR2_P377_R 47419933 NM_005534.2 3460 21 33696695 −377 Y
    IGF1_E394_F 19923111 NM_000618.2 3479 12 101398060 394 N
    IGFBP1_E48_R 61744448 NM_001013029.1 3484 7 45894532 48 Y
    IGFBP1_P12_R 61744448 NM_001013029.1 3484 7 45894472 −12 Y
    IGFBP5_P9_R 46094066 NM_000599.2 3488 2 217268525 −9 Y
    IL17RB_P788_R 27477073 NM_018725.2 55540 3 53854824 392 Y
    IL1RN_E42_F 27894320 NM_173843.1 3557 2 113591983 42 N
    IL1RN_P93_R 27894320 NM_173843.1 3557 2 113591848 −93 N
    INSR_P1063_R 4557883 NM_000208.1 3643 19 7246074 −1063 Y
    IPF1_P234_F 4557672 NM_000209.1 3651 13 27391943 −234 Y
    JAK3_P1075_R 47157314 NM_000215.2 3718 19 17820875 −1075 N
    KCNK4_E3_F 15718764 NM_016611.2 50801 11 63815454 3 Y
    KCNK4_P171_R 15718764 NM_016611.2 50801 11 63815280 −171 N
    KIAA1804_P689_R 24308329 NM_032435.1 84451 1 231529448 −689 Y
    KIT_P367_R 4557694 NM_000222.1 3815 4 55218551 −367 Y
    KLK10_P268_R 22208981 NM_002776.3 5655 19 56215362 −268 N
    KRAS_E82_F 34485724 NM_033360.2 3845 12 25295039 82 Y
    L1CAM_P19_F 13435352 NM_024003.1 3897 X 152794524 −19 Y
    LEFTY2_P561_F 27436880 NM_003240.2 7044 1 224196104 −561 N
    LOX_P313_R 21264603 NM_002317.3 4015 5 121442166 −313 Y
    LY6G6E_P45_R 13236491 NM_024123.1 79136 6 31789613 −1499 N
    LYN_P241_F 4505054 NM_002350.1 4067 8 56954685 −241 Y
    MAGEC3_E307_F 20162567 NM_138702.1 139081 X 140754075 307 N
    MAGEC3_P903_F 20162567 NM_138702.1 139081 X 140752865 −903 N
    MAP3K1_E81_F 88983555 XM_042066.10 4214 5 56146103 81 Y
    MAP3K1_P7_F 88983555 XM_042066.10 4214 5 56146015 −7 Y
    MAP3K8_P1036_F 22035597 NM_005204.2 1326 10 30761836 −1036 Y
    MAPK4_E273_R 6715608 NM_002747.2 5596 18 46444109 273 N
    MEST_E150_F 29294638 NM_002402.2 4232 7 129913432 150 Y
    MEST_P4_F 29294638 NM_002402.2 4232 7 129913278 −4 Y
    MEST_P62_R 29294638 NM_002402.2 4232 7 129913220 −62 Y
    MET_E333_F 42741654 NM_000245.2 4233 7 116100028 333 Y
    MMP7_E59_F 75709180 NM_002423.3 4316 11 101906629 59 N
    MPO_P883_R 4557758 NM_000250.1 4353 17 53714178 −883 N
    MST1R_E42_R 4505264 NM_002447.1 4486 3 49916032 42 Y
    MUC1_E18_R 65301116 NM_002456.4 4582 1 153429306 18 N
    NBL1_E205_R 33519445 NM_005380.3 4681 1 19842518 205 N
    NBL1_P24_F 33519445 NM_005380.3 4681 1 19842289 −24 N
    NOTCH4_E4_F 55770875 NM_004557.3 4855 6 32299818 4 N
    OPCML_P71_F 59939898 NM_002545.3 4978 11 132907684 −71 N
    PARP1_P610_R 11496989 NM_001618.2 142 1 224663024 −610 Y
    PDGFRA_E125_F 61699224 NM_006206.3 5156 4 54790329 125 N
    PDGFRB_E195_R 68216043 NM_002609.3 5159 5 149515420 195 N
    PGR_P790_F 31981491 NM_000926.2 5241 11 100507255 −790 N
    P13_P1394_R 31657130 NM_002638.2 5266 20 43235518 −1394 N
    PLAU_P176_R 53729348 NM_002658.2 5328 10 75340720 −176 Y
    POMC_P400_R 4505948 NM_000939.1 5443 2 25245356 −400 Y
    PRSS1_E45_R 21071011 NM_002769.2 5644 7 142136949 45 N
    PRSS1_P1249_R 21071011 NM_002769.2 5644 7 142135655 −1249 N
    PRSS8_E134_R 21536453 NM_002773.2 5652 16 31054518 134 Y
    PTHR1_P258_F 39995096 NM_000316.2 5745 3 46893982 −258 N
    PTK7_E317_F 27886610 NM_002821.3 5754 6 43152324 317 Y
    PTPN6_E171_R 34328901 NM_080548.2 5777 12 6926172 171 Y
    PTPRO_P371_F 13677212 NM_002848.2 5800 12 15366383 −371 N
    RARA_E128_R 75812906 NM_000964.2 5914 17 35719100 128 N
    RARA_P176_R 75812906 NM_000964.2 5914 17 35718796 −176 N
    RARB_E114_F 14916495 NM_016152.2 5915 3 25444872 114 Y
    RARB_P60_F 14916495 NM_016152.2 5915 3 25444698 −60 Y
    RARRES1_P426_R 46255042 NM_206963.1 5918 3 159933395 −426 Y
    RARRES1_P57_R 46255042 NM_206963.1 5918 3 159933026 −57 Y
    RBP1_P426_R 8400726 NM_002899.2 5947 3 140741606 −426 Y
    RIPK1_P744_R 57242760 NM_003804.3 8737 6 3021313 −744 N
    RIPK3_P124_F 40254843 NM_006871.2 11035 14 23879137 −124 N
    RUNX3_E27_R 72534651 NM_001031680.1 864 1 25164035 27 N
    RUNX3_P247_F 72534651 NM_001031680.1 864 1 25164309 −247 Y
    S100A2_P1186_F 45269153 NM_005978.3 6273 1 151806116 −1186 N
    SEMA3A_P343_F 5174672 NM_006080.1 10371 7 83662191 −343 N
    SEMA3A_P658_R 5174672 NM_006080.1 10371 7 83662506 −658 N
    SEMA3B_E96_F 54607087 NM_004636.2 7869 3 50280140 96 N
    SEMA3B_P110_R 54607087 NM_004636.2 7869 3 50279934 −110 N
    SERPINA5_P156_F 34147643 NM_000624.3 5104 14 94117408 −156 N
    SERPINE1_E189_R 10835158 NM_000602.1 5054 7 100557361 189 Y
    SHB_P691_R 4506934 NM_003028.1 6461 9 38059901 −691 Y
    SNCG_E119_F 4507112 NM_003087.1 6623 10 88708514 119 N
    SNCG_P53_F 4507112 NM_003087.1 6623 10 88708342 −53 Y
    SNCG_P98_R 4507112 NM_003087.1 6623 10 88708297 −98 Y
    SNURF_E256_R 29540557 NM_005678.3 8926 15 22751484 256 Y
    SPDEF_P6_R 6912579 NM_012391.1 25803 6 34632075 −6 N
    SPP1_E140_R 38146097 NM_000582.2 6696 4 89115966 140 N
    STAT5A_P704_R 21618341 NM_003152.2 6776 17 37692387 −704 N
    SYBL1_P349_F 27545446 NM_005638.3 6845 X 154763858 −349 Y
    TAL1_E122_F 4507362 NM_003189.1 6886 1 47467908 122 Y
    TAL1_P594_F 4507362 NM_003189.1 6886 1 47468624 −594 Y
    TEK_E75_F 4557868 NM_000459.1 7010 9 27099516 75 N
    TFF2_P178_F 48928025 NM_005423.3 7032 21 42644354 −178 N
    TGFB2_E226_R 4507462 NM_003238.1 7042 1 216586717 226 Y
    TGFB3_E58_R 4507464 NM_003239.1 7043 14 75517184 58 N
    TGFBI_P173_F 4507466 NM_000358.1 7045 5 135392424 −173 Y
    THBS2_P605_R 40317627 NM_003247.2 7058 6 169396667 −605 N
    THY1_P149_R 19923361 NM_006288.2 7070 11 118799239 −149 Y
    TNFRSF10A_P171_F 21361085 NM_003844.2 8797 8 23138755 70 Y
    TNFRSF10A_P91_F 21361085 NM_003844.2 8797 8 23138675 −10 Y
    TNFRSF10C_E109_F 22547120 NM_003841.2 8794 8 23016488 109 Y
    TNFRSF10C_P7_F 22547120 NM_003841.2 8794 8 23016372 −7 Y
    TNFRSF10D_E27_F 42544227 NM_003840.3 8793 8 23077458 27 Y
    TNFRSF10D_P70_F 42544227 NM_003840.3 8793 8 23077555 −70 Y
    TNFSF10_E53_F 23510439 NM_003810.2 8743 3 173723910 53 N
    TNFSF10_P2_R 23510439 NM_003810.2 8743 3 173723965 −2 N
    TNFSF8_E258_R 24119162 NM_001244.2 944 9 116732333 258 N
    TNFSF8_P184_F 24119162 NM_001244.2 944 9 116732775 −184 Y
    TNK1_P221_F 4507610 NM_003985.1 8711 17 7224913 −221 Y
    TRIM29_P261_F 17402908 NM_012101.2 23650 11 119514334 −261 N
    TRIP6_P1090_F 23308730 NM_003302.1 7205 7 100301891 −1090 Y
    VAV1_E9_F 7108366 NM_005428.2 7409 19 6723731 9 Y
    WNT10B_P823_R 16936521 NM_003394.2 7480 12 47652633 −823 Y
    Probe_ID SEQ ID Input_Sequence
    AATK_E63_R 94 GGGCAGAAGCCAGCTTGATGGCAGACACCT[CG]CCACCAGTAGCAGGCGTGGGAGAGTC
    AATK_P519_R 95 GGGGACGTGCCCAGTGGGTCCT[CG]AAGAAGGCAGGACAGAAGGCGG
    AATK_P709_R 96 ACGGGTGGCCCGTGGCCCAGCAG[CG]GCTCCATGGCCAGCGAGGCGG
    ALOX12_E85_R 97 GGGGCCTGGCTCTTCTCCGGGT[CG]TACAACCGCGTGCAGCTTTGGCTGGTCGG
    ALOX12_P223_R 98 CCGTTGGCCTCACCCTGGCT[CG]GGCCCCTTTATCATCCTGCAGCTACG
    ASCL2_P360_F 99 CCTAGCGCAGCTATGTCCCGAG[CG]CGCCCCCACCTGTGCGTTAATCTACTGG
    ASCL2_P609_R 100 GGGCCTGGAGGTCTGCACCCGAC[CG]CCTTGTGCCAGGACGGTCAGGT
    AXL_P223_R 101 GCCAGTAGCATGCCCCTGCC[CG]TCTGGGTCCCTCTGCGTGTCTCTGCTTGTC
    B3GALT5_E246_R 102 CACACTCCTGGCATCCCAG[CG]TCTCCAGCTTGCATGGCCTGTCACGGTATT
    BGN_P333_R 103 CCATCTCTCTTTCCTCTGCCTGG[CG]AGATGCCAGCCAGCACCTCAGTGTC
    BLK_P14_F 104 GACAAAGCAAAACCAGTGAGGCTGAAAGAA[CG]GCTGCCCTGGTGCACACAGATGG
    BMP4_P123_R 105 CCCGGAAGCCCAGGCAGCGCCCGAGTC[CG]CAGCTGCCGTCGGAGCTGGG
    BMP4_P199_R 106 GGGGCTCACCTGGGGACCACGTG[CG]GAGGTACTAGAAAGCATGCACCGACT
    CALCA_P171_F 107 AGGGGTCCTTTGCCCCTGGGTTG[CG]TCACCCTCATGCTTCCAGAACCTG
    CAPG_E228_F 108 CTTTCTTCCTCCTACCTCTGCTT[CG]TAGGTTCGTCTTCCTTCCAGCCTGC
    CASP10_E139_F 109 TTTGTTTTCAGGCAATTTCCCTGAGAAC[CG]TTTACTTCCAGAAGATTGGTGGAG
    CASP10_P334_F 110 TGTGGACATAAGAAAGGGTTAACATGGC[CG]ACAACTATTTCATGAGCTTTTTGGCTT
    CDH11_E102_R 111 GAGGGTGGACGCAACCTCCGAGC[CG]CCAGTCCCTGGCGCAGGGCAAGCG
    CDH11_P354_R 112 TCAGGGCTCAGATGGAGTCTGGAG[CG]ACTGAAGTTGGGCTCCAGGG
    CDH13_P88_F 113 CCGTATCTGCCATGCAAAACGAGGGAG[CG]TTAGGAAGGAATCCGTCTTGTAA
    CFTR_P372_R 114 TCTAGGAAGCTCTCCGGGGAGC[CG]GTTCTCCCGCCGGTGGCTTCTTCTG
    COL1A2_E299_F 115 ACCCTAGGGCCAGGGAAACTTTTGC[CG]TATAAATAGGGCAGATCCGGGCTTT
    COL1A2_P407_R 116 CAAAGCCTATCCTCCCTGTAGC[CG]GGTGCCAAGCAGCCTCGAGCCTGCTC
    COL1A2_P48_R 117 GACTGGACAGCTCCTGCTTTGATCGC[CG]GAGATCTGCAAATTCTGCCCATGTCGGGG
    CPA4_E20_F 118 CTTGACTCAGCCACTGTATGACTGACTCCC[CG]GGGACATGAGGTGGATACT
    CRIP1_P274_F 119 AGACATCACAGCGCTGGGCTAGGGGCG[CG]GCTTGAACTCGCCTAAAGAGCTG
    CRIP1_P874_R 120 CCTCAACTTTGCAGCGTACTTGGAC[CG]CTCTGGCCGCCCTGGGCGCTACCC
    CSF1R_P73_F 121 TCTAGCAGCTGCCTGTCACAGAGCA[CG]CCGGCCTCAATCCGGGCCTGTGGGC
    CSF3R_P8_F 122 GCTTCTCTCCCCGAGCTCTGT[CG]TTAATGGCTCAGCCTCTGACAGGCCCG
    CYP1B1_E83_R 123 GTTGAGATTGAGACTGGGGGT[CG]GTGAGTGGCGTCAATTCCCATG
    DDR1_P332_R 124 GGCCTGGGCGTCTGGACCCC[CG]GGTCCCTTAGAACGCCCTTCAGA
    DDR2_E331_F 125 GCGTTTTAAGTCAGACAAGGAAGGGAA[CG]TAATGAGGCACCACAGACTCGAGAAAT
    DDR2_P743_R 126 TCCTCCCCTGTTGCCTACC[CG]CCCCTTTCACATGATCTCTGACTATAGCTG
    DSC2_E90_F 127 CTGCGCAAGGTGTTTCTCACCAG[CG]GACGCCACCTATAAGGCCCATCTC
    ELK3_P514_F 128 GGCCGAGGGCTGGCTTTTAAAACAC[CG]AAAACCCAGACAGGAACGGTGTCC
    ELL_P693_F 129 ATCCCCACAGTCCCTGAG[CG]ATGGTGCAGTCCAGCTTCATTTTCCTATT
    EMR3_E61_F 130 AGCAAACTGCTTCCCCTCTTT[CG]CCATCAGACTCATGGTTCTGCTTTTCGTTT
    EVI2A_P94_R 131 CATGACAGGAGGCTTTGTAGAACCAATCCC[CG]CCTCCAGAGCAGGGAGGGTTTT
    EYA4_P794_F 132 TCAGCAATGTGCCTAGAGAAGCTCTGACGC[CG]CCTTGGAAGTAAGTCGTTGCTG
    FANCE_P356_R 133 CATGACAAGCAACATGCCGTCAG[CG]TAAATACAGCGCGGGTCCTCTAGCACA
    FGF9_P862_R 134 GACTCAGGGTTTCTTCCTCC[CG]CCTCTCGCAGTGCATCTTTCATTTGCTTTT
    FGFR1_P204_F 135 CTACAGCCTGGTCTCCTTTGGCGTTTG[CG]CCCCTGCATCTGAGCACGTCCCA
    FLT1_P615_R 136 GAAGTCTAGGAAGGCACCGGAGACCCT[CG]GCACAAGGCACTGAACCTGGAGCG
    FRZB_E186_R 137 CAGGATGGGGCAGGGTGCAGCCG[CG]CAGTGGACGCCAAAAGGCCCGCT
    FRZB_P406_F 138 GGGACGTCTGTGCCTCTGCCCGGG[CG]GCTCTGCACTTTCCTACCTCCCGC
    GFI1_P208_R 139 GAG GTCATACCCAGGCACTGGGTGTTGG[CG]GGAGCAGTAAAGCGCCATAAAAGCACC
    GJB2_P791_R 140 GTGCCAAGGACTAAGGTTGGGGG[CG]GTGGGAGAGACAAGCCTCGTT
    GJB2_P931_R 141 GGAACTGCAAGGAGGTGACTCCTTT[CG]GGGTGAGGAGGCCCAGAC
    GNMT_P197_F 142 GGGATTGCACAGAGGGCTGGGTC[CG]CAGGCTGGCTAAAAGGACCTAGCCC
    GP1BB_P278_R 143 ACACGATGCTCCGTTTTCTTC[CG]TTGTGAATGCCGCGTCCTGTCCTGGTGACA
    GRB10_P496_R 144 TACTCTGTCGTGGGCTGAAGGCACC[CG]GCCTGGGAAAAGGAAACC
    GRB7_E71_R 145 GCCTCTGACTTCTCTGTCCGAAGT[CG]GGACACCCTCCTACCACCTGTAGAG
    GRB7_P160_R 146 GGTACTGTCTGTTCGGCTGTCTTCCC[CG]CCTCTCCCCAGGCACCTGCATC
    GRPR_P200_R 147 CACATGGACACCCTGTGCATCAGTGTG[CG]TTTAATTCAAAGACAGACCTCATTTGATAG
    HBII-52_E142_F 148 GGCCCCCGACGGGGCCACTGTATTT[CG]GGCTGCAGACCTAGAGGCCCTG
    HBII-52_P563_F 149 GCCCAGGGGCAGGCTATGTGACTGCC[CG]GTCTGCAGCTGTAAGTGGTTTCT
    HCK_P858_F 150 TGGTGTCTGAATGGAGCAGGCCTG[CG]GAAGAGAAACCGCTGACCACAGACC
    HDAC7A_P344_F 151 AGCCTCACAGGCCCTCTGGGT[CG]CCACCCTCCCATGCTCTATCCC
    HFE_E273_R 152 TCCTCCTGATGCTTTTGCAGACCG[CG]GTCCTGCAGGGGCGCTTGCTGCGTGAGTCC
    HHIP_P578_R 153 AAACCATCTCAGCCTACTCAA[CG]GCATCTGGGATGTCCCCCTGCCTCTA
    HOXA11_E35_F 154 ACCTTGGGCTCTCCGCAGTAGC[CG]AGCTTAACATGATTCTCCACTGCAGCTGCC
    HOXA11_P92_R 155 CAGGGAGGTGCTGGTCATGTGACC[CG]ATGTTGAAATTGACAAGCTGCTAGCT
    HOXA9_E252_R 156 TGGGTTCCACGAGGCGCCAAACACCGT[CG]CCTTGGACTGGAAGCTGCACG
    HOXA9_P1141_R 157 CTACAAGTGGCATGAATGGAAGGCAAGTT[CG]GTTTGGGAAAAGGCAGCCTC
    HOXA9_P303_F 158 CCCCATACACACACTTCTTAAG[CG]GACTATTTTATATCACAATTAATCACGCCA
    HTR2A_P853_F 159 CCTGTTGGCTTCCTCTGGCACGGCT[CG]GCTGGGTTCCTCCCTCCCTGTGCGG
    IFNG_E293_F 160 AGCCTATCAGAGATGCTACAGCAAGT[CG ]ATATTCAGTCATTTTCAACCACAAA
    IFNGR2_P377_R 161 CTATGTTGCAAAACCCATTTTTGCTAA[CG]TGTCCAGTGGGCTCCCGGGACGAC
    IGF1_E394_F 162 TGTGCAAATGCATCCATCTCCC[CG]AGCTATTTTTCAGATTCCACAGAATTGCA
    IGFBP1_E48_R 163 ATTTTGAACACTCAGCTCCTAGCGTG[CG]GCGCTGCCAATCATTAACCTCCTGGTGC
    IGFBP1_P12_R 164 CCTCCCACCAGCGGTTTG[CG]TAGGGCCTTGGGTGCACTAGCAAAACAAAC
    IGFBP5_P9_R 165 GAAGTTTCCAAAGAGACTACGGGGCTC[CG]GGAGAGCAGGCGCTTTTAAATAGC
    IL17RB_P788_R 166 CAGCTCCAAATCGCCAGTGCTGA[CG]GCTTCCGCTTTGGGAGCCCCAG
    IL1RN_E42_F 167 GAGGGACTGTGGCCCAGGTACTGCC[CG]GGTGCTACTTTATGGGCAGCAGCT
    IL1RN_P93_R 168 CATCAAGTCAGCCATCAGC[CG]GCCCATCTCCTCATGCTGGCCAAC
    INSR_P1063_R 169 GACGCTTCTGAAAGGGCAAAGACGA[CG]CCAAAGAAGACGCCGGAGACCTC
    IPF1_P234_F 170 CCATTTTGGGGAGCACCGCCAGCTGCC[CG]TTCAGGAGTGTGCAGCAAACTCAGCTG
    JAK3_P1075_R 171 GGACAGGCACAGACTGGAACTTGGACC[CG]AGGCAGGACAGGGAGCTGGC
    KCNK4_E3_F 172 GAGATGCCAGATTAGCGTGGTGCCTGTC[CG]GAGAGACGGGCCAGCTGATG
    KCNK4_P171_R 173 AGGTGGGTCCCAACCTCCA[CG]TCGGCCAATTCCAGGTGGCCCC
    KIAA1804_P689_R 174 GCACTGGCCCAGGTCTGGCAC[CG]CGCTACAATTTCTTCTGTAGCCCGTTCTGA
    KIT_P367_R 175 GCGTGGTGCCCAGCTTCACAAAG[CG]AGCGGGCAGCACCTCCTTGGTCCG
    KLK10_P268_R 176 AACAGAAACAAGGAAAAAGGGAAACCCA[CG]CCCACTCTGTGGCCGTGAGTGA
    KRAS_E82_F 177 TCGCTCCCAGTCCGAAATGG[CG]GGGGCCGGGAGTACTGGCCGAGCCGC
    L1CAM_P19_F 178 CAGCACAGCCAGCCGGGCT[CG]GTTCAGGCTCCGGCCGGAGGGG
    LEFTY2_P561_F 179 CCCATGACATCCTCTGTCTAGACA[CG]GTCAGGACACAAATCTGGCAGCTCTACTGT
    LOX_P313_R 180 AGGCGAAGGCAGCCAGGCCATGGGG[CG]ACGCCAAAATATGCACGAAGAAAAATG
    LY6G6E_P45_R 181 AATCTGGGAGAGGTGATCTGCACCC[CG]AGATCCCGGGATTTGTAGAGTT
    LYN_P241_F 182 GGAAAGGAGACGCGAGAGGTGTAGT[CG]ATGTGCCTGCGAAGCCCAGGCT
    MAGEC3_E307_F 183 TCCCTTGGTTGCAGTAGCCTGTGGT[CG]CTCATGTCTGAATCTCCAGGGAA
    MAGEC3_P903_F 184 TGCAGCCTGAGTTAGACTTCTGCAACGTCC[CG]TGAGGTGGGATCAGGAATG
    MAP3K1_E81_F 185 CTGCAGGGAAGAAGGACGTGCGG[CG]AGAAGCATCGGATTCGGGG
    MAP3K1_P7_F 186 GTAGAGTCCAGGGACTAGGAGGACTCACAA[CG]CAGCGATGGGCAGCCAGGCCCTG
    MAP3K8_P1036_F 187 ACCTGGGCACTGGGAAGAATAGGG[CG]TGGACTTGGAGTGTGACCG
    MAPK4_E273_R 188 CCCTCCCAATGCAGGTTAAGA[CG]ACAGCCTGCGCCCCCAACTAGC
    MEST_E150_F 189 TCAGGAAGCGCATGCGCAACCGGTTCTC[CG]AAACATGGAGTCCTGTAGGCAAGG
    MEST_P4_F 190 GCTGACGCCTGGCAGGGAGAAGG[CG]GCAGCACATGCTGGGCTCGGG
    MEST_P62_R 191 GCCGGAGGCTATTGTCGAAGCCA[CG]GCCTGCCATTTCATACCCTTTGCAA
    MET_E333_F 192 GGAAACTGAAGAGACGTGGCCACGG[CG]AGGACGAAACTAGAATGGGG
    MMP7_E59_F 193 CAGGCACACAGCACACAGCA[CG]GTGAGTCGCATAGCTGCCGTCCAGAGAC
    MPO_P883_R 194 GGACAGGAAATCTGGCTGGAGAC[CG]TTGGGCTTCACAGGAAGGAG
    MST1R_E42_R 195 AGCAGCAACAGGAAGGACTGAGGCAGCGG[CG]GGAGGAGCTCCATCGAGGC
    MUC1_E18_R 196 GGAGGGGGCAGAACAGATTCAGGCAGG[CG]CTGGCTGCTTGAGAGGTG
    NBL1_E205_R 197 AAATCCCCAAGTCCTACAAT[CG]TGTCCCAGTGGTGTCCCTGGGCCAC
    NBL1_P24_F 198 GAATTCCGGGCAGAGGGAAGGG[CG]CAGGCAACAGCTAGGAGGCGCAGATGC
    NOTCH4_E4_F 199 CCTCGGCCTGCTGCAAGCCTCA[CG]TCTGAGCTGTTTCCTGAGTCACACAATGTC
    OPCML_P71_F 200 CAGAGCAGTCCTCCAAGGCA[CG]CATTGGCTCCACTCTCCTGAGCGACGG
    PARP1_P610_R 201 TCCGGGAAGCGCAGGCCCCCGCCT[CG]GGAATATAGTTGATTGGCCCGA
    PDGFRA_E125_F 202 GTGTGGGACATTCATTGCGGAATAACAT[CG]GAGGAGAAGGTAAGGGAA
    PDGFRB_E195_R 203 AAGCATCCTTCGGGAGGAGCAGAGC[CG]CCAGAGGGGCCGCCCTGG
    PGR_P790_F 204 CACTAGCAGTTATTCCACATTTC[CG]CCTAAATCTCCCAGCAGCCACTAATAT
    PI3_P1394_R 205 AAAGGCTTCCACAGTCTGACATT[CG]TTTATGTCTCCCTCAGTTTCAGGCTTGG
    PLAU_P176_R 206 TCTCGATTCCTCAGTCCAGA[CG]CTGTTGGGTCCCCTCCGCTGGAGATC
    POMC_P400_R 207 TGGTTCGCATTTGGCGGTAAATATCAC[CG]TCTGCACACGGGGAGGCCTCC
    PRSS1_E45_R 208 CTGATCCTTACCTTTGTGGCAGCTGCT[CG]TGAGTATCATGCCCTGCCTCAGGCCC
    PRSS1_P1249_R 209 TAGCCCCCTGGCCAGGTC[CG]ATTTCAACACCAAGTTTCTGAGCTTTT
    PRSS8_E134_R 210 GGGAGACGCCTGGAGTATCCGAAG[CG]AGCAGTGTGGACGAGTCACCAGCACCG
    PTHR1_P258_F 211 GGCAAGGAGAGGACTATTGAGGCACACACA[CG]TGTCTGGCAGCCTGAGTGGG
    PTK7_E317_F 212 GGGGGCACAGAGCTTGGGAAGCG[CG]GGAGTCCCGTGGGCAAAAG
    PTPN6_E171_R 213 GAGATGCTGTCCCGTGGGTAAGTCC[CG]GGCACCATCGGGGTCCCAGTCT
    PTPRO_P371_F 214 TGAGAGGGAACTGGGATCTGG[CG]CCTGGATTGCTCAAGAGAGGTC
    RARA_E128_R 215 CCCTTCCCAATTCTTTGGC[CG]CCTTTGACCCCGGCCTCTGCTTCTGA
    RARA_P176_R 216 GAACTGTTCCTGTCCCCAGC[CG]ATGACCAGACGCCCATCTTTCTTC
    RARB_E114_F 217 GAGGACTGGGATGCCGAGAACG[CG]AGCGATCCGAGCAGGGTTTGTC
    RARB_P60_F 218 CTAGTTGGGTCATTTGAAGGTTAGCAGCC[CG]GGTAGGGTTCACCGAAAGTTCA
    RARRES1_P426_R 219 CGGAGAAAGGGGCAGGCCGCAG[CG]GGCATTGATGGGGCTCCT
    RARRES1_P57_R 220 CCAGGGCGAAGGTCTGTAGCGAGCC[CG]GGTCCCCATGGGGCCACTCC
    RBP1_P426_R 221 GAAAGCTGGGAGGTTCAACTACGGG[CG]AGAAAATTGGGGCACTTTCCACG
    RIPK1_P744_R 222 CCCCTGTGTGAGCTACTGCCTGCCTC[CG]GTGCTCTGTTTCTGTCCCTAGAGTTCTTTT
    RIPK3_P124_F 223 AAAGCTAGTGCCTTTCTCCTTGACTAG[CG]TTTCCTGAGCACCTGCCGCAGCC
    RUNX3_E27_R 224 CGGCAGCCAGGGTGGAGGAGCTC[CG]AAGCTGACAGAGCAGAGTGGGCC
    RUNX3_P247_F 225 CGGCCTTGGCTCATTGGCTGGGCCG[CG]GTCACCTGGGCCGTGATGTCACGGCC
    S100A2_P1186_F 226 TCTACACCTTGGCACAGCCAC[CG]AGTGTCCCTTGCTCCCCTCAGTACTT
    SEMA3A_P343_F 227 CCTTTTATCTAAGCTCCTCTGATAGC[CG]GTGGCAGTCTCTAATCCTGCTCCCTGCTTC
    SEMA3A_P658_R 228 GAGATTAGAGCCGGGAGCAGAACCCTCAGG[CG]TGCCTGTGAAAGGCATGTAGCTATAA
    SEMA3B_E96_F 229 GAGAGATGCTGCTGCGGAAGTCCT[CG]GTGGAGTGTGAGAAGGCAGC
    SEMA3B_P110_R 230 CTTGTGCCCATTCCACTCC[CG]CCTGGCTGCCGTCTCCAGCTGGTCCC
    SERPINA5_P156_F 231 GCGTCTGCAGGCAGGCCTGCTGGC[CG]GAAACCTGCCAGGAAAGGAAG
    SERPINE1_E189_R 232 CGCTATTCCTCTATTTTCTTTTCCT[CG]GACCTGCAGCCTTGGGTCGACCCTGC
    SHB_P691_R 233 GGTGGGAGCCGGGCCCAGCACCAATC[CG]AGAGCAAGGCTAGGGGAGGTC
    SNCG_E119_F 234 GGAAAAGACCAAGCAGGGGGTGA[CG]GAAGCAGCTGAGAAGACCAAGGAG
    SNCG_P53_F 235 CGTCAATAGGAGGCATCGGGGACAGC[CG]CTGCGGCAGCACTCGAGCCAGCTCAAG
    SNCG_P98_R 236 GCTGGCTGGGCTCCAGCTGGCCTC[CG]CATCAATATTTCATCGGCGTCAATAGGA
    SNURF_E256_R 237 AGGCTTGCTGTTGTGCCGTTCTGCCC[CG]ATGGTATCCTGTCCGCTCGCATTGGGGCG
    SPDEF_P6_R 238 TGTGCTGGGAGGAAGTCAGACAGCCG[CG]AGATGAAGAGTTGGCCAGGGC
    SPP1_E140_R 239 AGTTGCAGCCTTCTCAGCCAAA[CG]CCGACCAAGGTACAGCTTCAGTTTGCTACT
    STAT5A_P704_R 240 CAGCCACCGACAGGCTGCATGA[CG]GTGGCAAAGTCACTTCCCCTCTCTG
    SYBL1_P349_F 241 ATTTTGTCTGTGAGGAAACGGG[CG]ACGCTGCCTACTGAGACTAAGCAGGA
    TAL1_E122_F 242 CCGACAGGCTGTCTGGAACATTTT[CG]AACCCTCCAACTGGGATCGGTCTGGTT
    TAL1_P594_F 243 TCACACATCGAAGTCTTGGATTAACTG[CG]AAGGCCTCCTTCTATTTGCCGCGGCTT
    TEK_E75_F 244 GTAGGACGATGCTAATGGAAAGTCACAAAC[CG]CTGGGTTTTTGAAAGGATC
    TFF2_P178_F 245 GCCAGGGTGACTCTCTCCCTGCT[CG]GTGATACCTCTTCCTGCCCTGGACAGA
    TGFB2_E226_R 246 TTTCTGATCCTGCATCTGGTCACGGT[CG]CGCTCAGCCTGTCTACCTGCAGCACACT
    TGFB3_E58_R 247 CAGGAAGCGCTGGCAACCCTGAGGA[CG]AAGAAGCGGACTGTGTGCCTT
    TGFBI_P173_F 248 ACTGAGCACGGGCACAGTGCGGGAG[CG]GGTGGGTGCCCAGGGCAG
    THBS2_P605_R 249 AACCTGACGTGCAGGCACAGAGCAAGGACT[CG]AGAGAACGAGAAGCAGTGGCAGCAGCT
    THY1_P149_R 250 GGAAGGAAGAGAAGGCGGTCC[CG]CATTGGTGTGAGAGTGGCAGG
    TNFRSF10A_P171_F 251 TCGTTTTGCCACTTGGTCCCAG[CG]CCAGGCTTCTCGGTCGGGAGTTGACCT
    TNFRSF10A_P91_F 252 TTCCTCTGTGACCGCCCTTGC[CG]CTCTCAGCTTCTGTTCCTCAACCAC
    TNFRSF10C_E109_F 253 AGGGGTGAAGGAGCGCTTCCTAC[CG]TTAGGGAACTCTGGGGACAG
    TNFRSF10C_P7_F 254 GGGTATAAATTCAGAGGCGCTGCGCTC[CG]ATTCTGGCAGTGCAGCTGTGGG
    TNFRSF10D_E27_F 255 CAGAAATCGTCCCCGTAGTTTGTG[CG]CGTGCAAAGGTTCTCGCAGCTACACTGCCA
    TNFRSF10D_P70_F 256 CGTGGTCAGTTGTACTCCCTTCC[CG]CAGTCACTTCCAGGCACTCAGGCTGG
    TNFSF10_E53_F 257 GACTGCTGTAAGTCAGCCAGGCAGC[CG]GTCACTGAAGCCCTTCCTTCTCTATT
    TNFSF10_P2_R 258 TCTTTTATAGTCAGTGAGGAAATGAAAG[CG]AATGAGTTGTTTTTCTGGGT
    TNFSF8_E258_R 259 CCCCAGGTGGCTGGCCACGGAGCC[CG]CCGGCACATGCATGGCTGTGTCTC
    TNFSF8_P184_F 260 CACACACAAAGCAACTTCTGTTT[CG]TTTAGACTCTGCCACAAAACGCCTTC
    TNK1_P221_F 261 GGCTGGAAAGACGTGAAGGAAGA[CG]AGCAGAGGAGAAGGGAAGG
    TRIM29_P261_F 262 GCACTTGCTTCTCATCCGGGGAG[CG]GGGAGTCTCCGTCTTCACAAGTGGGCA
    TRIP6_P1090_F 263 AAGGGGACTTTGTGAACAGTGGG[CG]GGGAGACGCAGAGGCAGAGG
    VAV1_E9_F 264 AAAGAAGAGGAAGTGGTAGCACTAGCTGT[CG]CTCCACAGGCGAGCAGGGCAGGCG
    WNT10B_P823_R 265 CTTGGGGTGCACAGGCAAAGGCAAAC[CG]CCTTAGGGAGACCCAGTGGCAGCG
    Probe_ID Synonym cg_no
    AATK_E63_R . cg05292376
    AATK_P519_R . cg17279079
    AATK_P709_R . cg02979355
    ALOX12_E85_R LOG12 cg05878700
    ALOX12_P223_R LOG12 cg22819332
    ASCL2_P360_F ASH2, HASH2, MASH2 cg15376678
    ASCL2_P609_R ASH2, HASH2, MASH2 cg00868120
    AXL_P223_R UFO cg09524393
    B3GALT5_E246_R B3T5, GLCT5, B3GalTx, B3GalT-V, beta3Gal-T5 cg11479877
    BGN_P333_R PGI, DSPG1, PG-S1, SLRR1A cg04929865
    BLK_P14_F MGC10442 cg22826986
    BMP4_P123_R ZYME, BMP2B, BMP2B1 cg26240298
    BMP4_P199_R ZYME, BMP2B, BMP2B1 cg09229893
    CALCA_P171_F CT, KC, CGRP, CALC1, CGRP1, CGRP-I, MGC126648 cg24117998
    CAPG_E228_F MCP, AFCP cg13268943
    CASP10_E139_F MCH4, ALPS2, FLICE2 cg20209903
    CASP10_P334_F MCH4, ALPS2, FLICE2 cg13782463
    CDH11_E102_R OB, CAD11, CDHOB, OSF-4 cg05318914
    CDH11_P354_R OB, CAD11, CDHOB, OSF-4 cg13126606
    CDH13_P88_F CDHH cg08977371
    CFTR_P372_R CF, MRP7, ABC35, ABCC7, TNR-CFTR, dJ76005.1 cg24329417
    COL1A2_E299_F OI4 cg22877867
    COL1A2_P407_R OI4 cg16337370
    COL1A2_P48_R OI4 cg26942275
    CPA4_E20_F CPA3 cg01796223
    CRIP1_P274_F CRHP, CRIP, CRP1 cg05417129
    CRIP1_P874_R CRHP, CRIP, CRP1 cg03324382
    CSF1R_P73_F FMS, CSFR, FIM2, C-FMS, CD115 cg01875467
    CSF3R_P8_F CD114, GCSFR cg00474419
    CYP1B1_E83_R CP1B, GLC3A cg09991178
    DDR1_P332_R CAK, DDR, NEP, PTK3, RTK6, TRKE, CD167, EDDR1, MCK10, NTRK4, PTK3A cg02680487
    DDR2_E331_F TKT, NTRKR3, TYRO10 cg22740835
    DDR2_P743_R TKT, NTRKR3, TYRO10 cg23028772
    DSC2_E90_F DG2, DSC3, CDHF2, DGII/III, DKFZp686I11137 cg08156793
    ELK3_P514_F ERP, NET, SAP2 cg11467837
    ELL_P693_F Men, ELL1, C19orf17, ELL_HUMAN, DKFZp434I1916 cg09597048
    EMR3_E61_F . cg15552238
    EVI2A_P94_R EVDA, EVI2 cg23352695
    EYA4_P794_F CMD1J, DFNA10 cg24842760
    FANCE_P356_R FAE, FACE cg04035266
    FGF9_P862_R GAF, HBFG-9, MGC119914, MGC119915 cg02259997
    FGFR1_P204_F H2, H3, H4, H5, CEK, FLG, FLT2, KAL2, BFGFR, C-FGR, CD331, N-SAM cg20658205
    FLT1_P615_R FLT, VEGFR1 cg26282369
    FRZB_E186_R FRE, FZRB, hFIZ, FRITZ, FRP-3, FRZB1, SFRP3, SRFP3, FRZB-1, cg01872931
    FRZB-PEN
    FRZB_P406_F FRE, FZRB, hFIZ, FRITZ, FRP-3, FRZB1, SFRP3, SRFP3, FRZB-1, cg25188149
    FRZB-PEN
    GFI1_P208_R ZNF163 cg20125091
    GJB2_P791_R HID, KID, PPK, CX26, DFNA3, DFNB1, NSRD1 cg20193013
    GJB2_P931_R HID, KID, PPK, CX26, DFNA3, DFNB1, NSRD1 cg09195389
    GNMT_P197_F . cg04013093
    GP1BB_P278_R CD42c cg19755554
    GRB10_P496_R RSS, IRBP, MEG1, GRB-IR, KIAA0207 cg19392396
    GRB7_E71_R . cg23836594
    GRB7_P160_R . cg08284496
    GRPR_P200_R . cg26196133
    HBII-52_E142_F RNHBII52 cg24301180
    HBII-52_P563_F RNHBII52 cg21361081
    HCK_P858_F JTK9 cg04775393
    HDAC7A_P344_F HDAC7, DKFZP586J0917 cg25755806
    HFE_E273_R HH, HFE1, HLA-H, MGC103790, dJ221C16.10.1 cg13740565
    HHIP_P578_R HIP, FLJ20992, FLJ90230 cg02524475
    HOXA11_E35_F HOX1, HOX1I cg08479590
    HOXA11_P92_R HOX1, HOX1I cg18977999
    HOXA9_E252_R HOX1, ABD-B, HOX1G, HOX1.7, MGC1934 cg10604830
    HOXA9_P1141_R HOX1, ABD-B, HOX1G, HOX1.7, MGC1934 cg15262939
    HOXA9_P303_F HOX1, ABD-B, HOX1G, HOX1.7, MGC1934 cg03715906
    HTR2A_P853_F HTR2, 5-HT2A cg15268261
    IFNG_E293_F IFG, IFI cg23001963
    IFNGR2_P377_R AF-1, IFGR2, IFNGT1 cg21449657
    IGF1_E394_F IGFI cg17084217
    IGFBP1_E48_R AFBP, IBP1, PP12, IGF-BP25, hIGFBP-1 cg20666158
    IGFBP1_P12_R AFBP, IBP1, PP12, IGF-BP25, hIGFBP-1 cg00110785
    IGFBP5_P9_R IBP5 cg20419545
    IL17RB_P788_R CRL4, EVI27, IL17BR, IL17RH1, MGC5245 cg16868427
    IL1RN_E42_F IRAP, IL1F3, IL1RA, IL-1ra3, ICIL-1RA, MGC10430 cg17669033
    IL1RN_P93_R IRAP, IL1F3, IL1RA, IL-1ra3, ICIL-1RA, MGC10430 cg14497465
    INSR_P1063_R CD220 cg00650214
    IPF1_P234_F IUF1, PDX1, IDX-1, MODY4, PDX-1, STF-1 cg20815612
    JAK3_P1075_R JAKL, LJAK, JAK-3, L-JAK, JAK3_HUMAN cg05244380
    KCNK4_E3_F TRAAK, DKFZP566E164 cg01352108
    KCNK4_P171_R TRAAK, DKFZP566E164 cg25881850
    KIAA1804_P689_R MLK4, dJ862P8.3 cg09524235
    KIT_P367_R PBT, SCFR, C-Kit, CD117 cg23927351
    KLK10_P268_R NES1, PRSSL1 cg06130787
    KRAS_E82_F KRAS1, KRAS2, RASK2, KI-RAS, C-K-RAS, K-RAS2A, K-RAS2B, K-RAS4A, cg26129757
    K-RAS4B
    L1CAM_P19_F S10, HSAS, MASA, MIC5, SPG1, CAML1, CD171, HSAS1, N-CAML1 cg12024667
    LEFTY2_P561_F EBAF, LEFTA, TGFB4, LEFTYA, MGC46222 cg22462235
    LOX_P313_R MGC105112 cg08623535
    LY6G6E_P45_R G6e, C6orf22 cg26399860
    LYN_P241_F JTK8 cg04283851
    MAGEC3_E307_F HCA2, MAGEC4, MAGE-C3, MGC119270, MGC119271 cg02818322
    MAGEC3_P903_F HCA2, MAGEC4, MAGE-C3, MGC119270, MGC119271 cg22177388
    MAP3K1_E81_F . cg00468724
    MAP3K1_P7_F . cg06448700
    MAP3K8_P1036_F COT, EST, ESTF, TPL2, TpI-2, c-COT, FLJ10486 cg21555918
    MAPK4_E273_R ERK3, Erk4, PRKM4, p63MAPK cg21612229
    MEST_E150_F PEG1, MGC8703, MGC111102, DKFZp686L18234 cg05241978
    MEST_P4_F PEG1, MGC8703, MGC111102, DKFZp686L18234 cg20632786
    MEST_P62_R PEG1, MGC8703, MGC111102, DKFZp686L18234 cg07409197
    MET_E333_F HGFR, RCCP2 cg24548568
    MMP7_E59_F MMP-7, MPSL1, PUMP-1 cg10521988
    MPO_P883_R . cg24997501
    MST1R_E42_R RON, PTK8, CDw136 cg03714052
    MUC1_E18_R EMA, PEM, PUM, MAM6, PEMT, CD227, H23AG, mucin cg00265953
    NBL1_E205_R NB, DAN, NO3, DAND1, MGC8972, D1S1733E cg21813747
    NBL1_P24_F NB, DAN, NO3, DAND1, MGC8972, D1S1733E cg04102045
    NOTCH4_E4_F INT3, NOTCH3, MGC74442 cg14700707
    OPCML_P71_F OPCM, OBCAM cg00738841
    PARP1_P610_R PARP, PPOL, ADPRT, ADPRT1, PARP-1, pADPRT-1 cg17303114
    PDGFRA_E125_F CD140A, PDGFR2, MGC74795 cg20629161
    PDGFRB_E195_R JTK12, PDGFR, CD140B, PDGFR1, PDGF-R-beta cg21817429
    PGR_P790_F PR, NR3C3 cg01987509
    PI3_P1394_R ESI, WAP3, SKALP, WFDC14, MGC13613 cg18675416
    PLAU_P176_R ATF, UPA, URK, u-PA cg26457761
    POMC_P400_R MSH, POC, ACTH, CLIP cg22632966
    PRSS1_E45_R TRP1, TRY1, TRY4, TRYP1, MGC120175 cg16567953
    PRSS1_P1249_R TRP1, TRY1, TRY4, TRYP1, MGC120175 cg09471643
    PRSS8_E134_R CAP1, PROSTASIN cg27436259
    PTHR1_P258_F PTHR, MGC138426, MGC138452 cg13804333
    PTK7_E317_F CCK4 cg21726633
    PTPN6_E171_R HCP, HCPH, SHP1, SHP-1, HPTP1C, PTP-1C, SHP-1L, SH-PTP1 cg00788854
    PTPRO_P371_F PTPU2, GLEPP1, PTP-U2 cg25816184
    RARA_E128_R RAR, NR1B1 cg00848035
    RARA_P176_R RAR, NR1B1 cg10363722
    RARB_E114_F HAP, RRB2, NR1B2 cg14265392
    RARB_P60_F HAP, RRB2, NR1B2 cg06720425
    RARRES1_P426_R TIG1 cg13848998
    RARRES1_P57_R TIG1 cg12199224
    RBP1_P426_R CRBP, RBPC, CRBP1, CRABP-I cg11986962
    RIPK1_P744_R RIP, FLJ39204 cg24303123
    RIPK3_P124_F RIP3, RIP3 beta, RIP3 gamma cg13583230
    RUNX3_E27_R AML2, CBFA3, PEBP2aC cg21368948
    RUNX3_P247_F AML2, CBFA3, PEBP2aC cg10672665
    S100A2_P1186_F CAN19, S100L, MGC111539 cg21074565
    SEMA3A_P343_F SemD, SEMA1, SEMAD, SEMAL, coll-1, Hsema-I, SEMAIII, sema III cg16346212
    SEMA3A_P658_R SemD, SEMA1, SEMAD, SEMAL, coll-1, Hsema-I, SEMAIII, sema III cg00927350
    SEMA3B_E96_F SemA, SEMA5, SEMAA, semaV, LUCA-1, FLJ34863 cg25047248
    SEMA3B_P110_R SemA, SEMA5, SEMAA, semaV, LUCA-1, FLJ34863 cg12999941
    SERPINA5_P156_F PCI, PAI3, PROCI, PLANH3 cg13984563
    SERPINE1_E189_R PAI, PAI1, PAI-1, PLANH1 cg10678915
    SHB_P691_R RP11-3J10.8 cg19574087
    SNCG_E119_F SR, BCSG1 cg26738310
    SNCG_P53_F SR, BCSG1 cg12027410
    SNCG_P98_R SR, BCSG1 cg03677069
    SNURF_E256_R . cg07995992
    SPDEF_P6_R PDEF, bA375E1.3, RP11-375E1_A.3 cg10159596
    SPP1_E140_R OPN, BNSP, BSPI, ETA-1, MGC110940 cg20261167
    STAT5A_P704_R MGF, STAT5 cg09355539
    SYBL1_P349_F VAMP7, VAMP-7, TI-VAMP cg11419984
    TAL1_E122_F SCL, TCL5, tal-1 cg00875272
    TAL1_P594_F SCL, TCL5, tal-1 cg13537642
    TEK_E75_F TIE2, VMCM, TIE-2, VMCM1, CD202B cg05749772
    TFF2_P178_F SP, SML1 cg10018784
    TGFB2_E226_R MGC116892, TGF-beta2 cg20490551
    TGFB3_E58_R FLJ16571, TGF-beta3 cg17928876
    TGFBI_P173_F CSD, CDB1, CDG2, CSD1, CSD2, CSD3, LCD1, BIGH3, CDGG1 cg00833799
    THBS2_P605_R TSP2 cg24654845
    THY1_P149_R CD90 cg18809507
    TNFRSF10A_P171_F DR4, APO2, CD261, MGC9365, TRAILR1, TRAILR-1 cg00990613
    TNFRSF10A_P91_F DR4, APO2, CD261, MGC9365, TRAILR1, TRAILR-1 cg25641272
    TNFRSF10C_E109_F LIT, DCR1, TRID, CD263, TRAILR3 cg05937208
    TNFRSF10C_P7_F LIT, DCR1, TRID, CD263, TRAILR3 cg23831143
    TNFRSF10D_E27_F DCR2, CD264, TRUNDD, TRAILR4 cg01031400
    TNFRSF10D_P70_F DCR2, CD264, TRUNDD, TRAILR4 cg04134048
    TNFSF10_E53_F TL2, APO2L, CD253, TRAIL, Apo-2L cg16555388
    TNFSF10_P2_R TL2, APO2L, CD253, TRAIL, Apo-2L cg27433414
    TNFSF8_E258_R CD153, CD30L, CD30LG cg09980061
    TNFSF8_P184_F CD153, CD30L, CD30LG cg19343707
    TNK1_P221_F MGC46193 cg26000767
    TRIM29_P261_F ATDC cg13907859
    TRIP6_P1090_F OIP1, ZRP-1, MGC3837, MGC4423, MGC10556, MGC10558, MGC29959 cg09357642
    VAV1_E9_F VAV cg02621492
    WNT10B_P823_R WNT-12 cg23890019
    • 6.13. Methylation Subgroup Analysis
  • Comparisons were also performed to show the relationship between several biological characteristics of the samples and the methylation profile. These methylation profiles may be used as a surrogate for measuring the biological characteristic, e.g., Breslow depth, when the location does not lend itself to such measurement, failure to annotate the sample, drug or treatment selection; selection of an appropriate combination of independent and additive conventional diagnostic markers to be used in conjunction with the methylation markers described in this application; or other reasons.
  • Specifically, Table 10 lists CpG methylation sites associated with Breslow depth. In addition, analysis to study mitotic rate (Table 11) and ulceration were performed. For ulceration, one methylation correlated significantly, ProbeID MAP3K1_P7_F with a p value of 0.00096. The results for Breslow depth, mitotic rate, and mutations are shown below.
  • TABLE 10
    CpG Methylation sites associated with Breslow depth
    ProbeID p.value.Breslow q.value.Breslow coef.Breslow mean.beta.adjusted
    ABCB4_E429_F 0.000151351 0.055067493 0.075844142 0.951470796
    GNG7_E310_R 0.000360298 0.101027535 0.064175387 0.963251731
    HOXA9_E252_R 0.000587998 0.137395588 0.289499517 0.706184222
    HOXA9_P303_F 4.68E−05 0.055067493 0.281051363 0.373700815
    IRAK3_P185_F 0.000157111 0.055067493 0.251012726 0.373687534
    PTK7_E317_F 0.000114644 0.055067493 0.16729955 0.341920543
    RUNX1T1_E145_R 0.000767285 0.153676131 0.217039165 0.415388499
  • TABLE 11
    CpG Methylation sites associated with mitotic rate (MitRate)
    ProbeID p.value.MitRate q.value.MitRate coef.MitRate mean.beta
    USP29_P282_R 0.000859842 0.674750416 −0.102118216 0.870617418
    SHH_P104_R 0.006076261 0.674750416 −0.070286692 0.095698924
    SEMA3A_P658_R 0.013545534 0.702374503 −0.144593294 0.462172928
    MMP14_P208_R 0.017198003 0.705774866 −0.094456225 0.180542789
    UGT1A7_P751_R 0.017395592 0.705774866 −0.060682502 0.952848615
    AATK_P709_R 0.038655609 0.74311075 −0.091648145 0.718552347
  • TABLE 12
    Analysis of CpG sites associated with mutation (Mut) for any mutation in BRAF
    codon 15, and NRAS codon 61. Nearly all of the mutation samples had mutations at BRAF
    V600. Thus, the sites below may be useful to select specific patients for therapy that are likely
    to respond because of the presence of BRAF mutations.
    ProbeID p.value.Mut.Uni q.value.Mut.Uni p.value.Mut.Multi q.value.Mut.Multi
    CCR5_P630_R 0.05511171 0.492144064 0.000689708 0.16766822
    CD40_E58_R 0.001758825 0.273985791 0.000717553 0.16766822
    DNMT3B_P352_R 0.001006177 0.230434732 0.000641606 0.16766822
    GPX1_P194_F 0.001592276 0.273985791 0.000201973 0.16766822
    KLK10_P268_R 6.22E−05 0.0872197 0.000400032 0.16766822
    P2RX7_E323_R 0.001008864 0.230434732 0.000663112 0.16766822
    SEMA3B_P110_R 0.001328043 0.267401202 0.000895024 0.240377935

    Table β shows the accession numbers; specific single CpG coordinate; presence or absence of CpG islands; specific sequences used in the Illumina GoldenGate array experiments; and the synonyms for genes hypermethylated or hypomethylated in the subset analysis. All gene IDs and accession numbers are from Ref. Seq. version 36.1.
  • Probe_ID Gid Accession Gene_ID CHRM CpG_Coor Dist_to_TSS CpG_i
    AATK_P709_R 89041906 XM_927215.1 9625 17 76710603 −709 Y
    ABCB4_E429_F 9961251 NM_018850.1 5244 7 86947255 429 N
    CD40_E58_R 23312370 NM_152854.1 958 20 44180371 58 Y
    DNMT3B_P352_R 28559060 NM_175848.1 1789 20 30813500 −352 N
    GNG7_E310_R 32698768 NM_052847.1 2788 19 2603280 310 Y
    HOXA9_E252_R 24497558 NM_002142.3 3205 7 27171422 252 Y
    HOXA9_P303_F 24497558 NM_002142.3 3205 7 27171977 −303 Y
    IRAK3_P185_F 6005791 NM_007199.1 11213 12 64869099 −185 Y
    KLK10_P268_R 22208981 NM_002776.3 5655 19 56215362 −268 N
    MAP3K1_P7_F 88983555 XM_042066.10 4214 5 56146015 −7 Y
    MMP14_P208_R 13027797 NM_004995.2 4323 14 22375425 −208 N
    PTK7_E317_F 27886610 NM_002821.3 5754 6 43152324 317 Y
    RUNX1T1_E145_R 28329418 NM_175635.1 862 8 93176474 145 N
    SEMA3A_P658_R 5174672 NM_006080.1 10371 7 83662506 −658 N
    SEMA3B_P110_R 54607087 NM_004636.2 7869 3 50279934 −110 N
    SHH_P104_R 21071042 NM_000193.2 6469 7 1.55E+08 −104 Y
    UGT1A7_P751_R 41282212 NM_019077.2 54577 2 2.34E+08 −751 N
    USP29_P282_R 56790915 NM_020903.2 57663 19 62323039 −282 Y
    SEQ
    Probe_ID ID Input_Sequence
    AATK_P709_R 266 ACGGGTGGCCCGTGGCCCAGCAG[CG]GCTCCATGGCCAGCGAGGCGG
    ABCB4_E429_F 267 TTCCTTGGACTTCTCAGTCTATTCT[CG]CCACTTCTGTCATGTCAGTCAGTCACAC
    CD40_E58_R 268 CGGGCGCCCAGTGGTCCTGC[CG]CCTGGTCTCACCTCGCTATGGTTCGTCTGC
    DNMT3B_P352_R 269 CTGCCCTCTCTGAGCCCC[CG]CCTCCAGGCCTGTGTGTGTGTCTCCGTTCG
    GNG7_E310_R 270 AGGCCAGACGCTGAGAGAGAAAAACACTG[CG]TAATCCCACGTATTGTGGAGTCCAAAA
    HOXA9_E252_R 271 TGGGTTCCACGAGGCGCCAAACACCGT[CG]CCTTGGACTGGAAGCTGCACG
    HOXA9_P303_F 272 CCCCATACACACACTTCTTAAG[CG]GACTATTTTATATCACAATTAATCACGCCA
    IRAK3_P185_F 273 CCCCACCGCAGAGGTGTGAAGGGG[CG]CAAAGCCAGCGAAGGGAGAACCCG
    KLK10_P268_R 274 AACAGAAACAAGGAAAAAGGGAAACCCA[CG]CCCACTCTGTGGCCGTGAGTGA
    MAP3K1_P7_F 275 GTAGAGTCCAGGGACTAGGAGGACTCACAA[CG]CAGCGATGGGCAGCCAGGCCCTG
    MMP14_P208_R 276 CTACAGCCCCCTGCTGTCCAT[CG]CGGCCTCAACCCCTGCAGATGGCA
    PTK7_E317_F 277 GGGGGCACAGAGCTTGGGAAGCG[CG]GGAGTCCCGTGGGCAAAAG
    RUNX1T1_E145_R 278 GGATAGCAGAGGTGATGGGAGATAG[CG]TCAAGGCCAGGGGTAGATGCCTC
    SEMA3A_P658_R 279 GAGATTAGAGCCGGGAGCAGAACCCTCAGG[CG]TGCCTGTGAAAGGCATGTAGCTATAA
    SEMA3B_P110_R 280 CTTGTGCCCATTCCACTCC[CG]CCTGGCTGCCGTCTCCAGCTGGTCCC
    SHH_P104_R 281 ATGGCAGGCTGCCGGCCGCTGATAA[CG]GAACACATCGGAGTTGGGTCG
    UGT1A7_P751_R 282 CGCTAAGACCCTTGCTCTCTTTC[CG]TCGAACATGAGATGCCAATTTCTTTCTGGG
    USP29_P282_R 283 TTTCTCTGAACCCTAACTCCTGC[CG]TTACGCCCCACCAGCTCTAGGCC
    Probe_ID Synonym cg_no
    AATK_P709_R . cg02979355
    ABCB4_E429_F MDR3, PGY3, ABC21, MDR2/3, PFIC-3 cg05279864
    CD40_E58_R p50, Bp50, CDW40, MGC9013, TNFRSF5 cg20698532
    DNMT3B_P352_R ICF, M. HsaIIIB cg14703690
    GNG7_E310_R FLJ00058 cg13502721
    HOXA9_E252_R HOX1, ABD-B, HOX1G, HOX1.7, MGC1934 cg10604830
    HOXA9_P303_F HOX1, ABD-B, HOX1G, HOX1.7, MGC1934 cg03715906
    IRAK3_P185_F IRAK-M cg24003063
    KLK10_P268_R NES1, PRSSL1 cg06130787
    MAP3K1_P7_F . cg06448700
    MMP14_P208_R MMP-X1, MTMMP1, MT1-MMP cg01508380
    PTK7_E317_F CCK4 cg21726633
    RUNX1T1_E145_R CDR, ETO, MTG8, MTG8b, AML1T1, ZMYND2, CBFA2T1, cg07538339
    MGC2796
    SEMA3A_P658_R SemD, SEMA1, SEMAD, SEMAL, coll-1, Hsema-I, SEMAIII, cg00927350
    sema III
    SEMA3B_P110_R SemA, SEMA5, SEMAA, semaV, LUCA-1, FLJ34863 cg12999941
    SHH_P104_R HHG1, HLP3, HPE3, SMMCI cg06981396
    UGT1A7_P751_R UDPGT, UGT1G, UGT1*7 cg16671505
    USP29_P282_R HOM-TES-84/86 cg16675193
    • 6.14. Methylation Specific PCR Examples
  • Sodium bisulfite modification and methylation-specific PCR (Method A): Digested DNA (500 ng) is denatured in 0.3 N NaOH at 37° C. for 15 min (Clark et al., 1994, Nucleic Acids Res. 22, 2990-2997). Then, 3.6 N sodium bisulfite (pH 5.0) and 0.6 mM hydroquinone are added, and the sample undergoes 15 cycles of 1) denaturation at 95° C. for 30 s and 2) incubation at 50° C. for 15 min. The sample is desalted with the Wizard DNA Clean-Up system (Promega, Madison, Wis.), and desulfonated in 0.3 N NaOH. DNA was ethanol-precipitated and dissolved in 20 n1 of buffer. Methylation-specific PCR (MSP) is performed with a primer set specific to the methylated or unmethylated sequence (M or U set), using 0.5 μl of the sodium-bisulfite-treated DNA (Herman et al., 1996, Proc. Natl. Acad. Sci. USA, 93, 9821-9826). Primers and probes are designed based on the sequences shown in Table 4. the Zymo Universal Methylated DNA Standard is used as the positive, fully-methylated control, and a GenomePlex (Sigma) whole genome amplified (WGA) DNA is used as the negative, unmethylated control.
  • Sodium Bisulfite DNA Treatment (Method B):
  • DNA is sodium bisulfite treated using the EZ DNA Methylation-Gold Kit (Zymo Research, cat. #D5005). The DNA sample (˜10-20 ul lysate or 200-500 ng DNA) is mixed with 130 ul of CT Conversion Reagent in a PCR tube and denatured in a thermal cycler at 98° C. for 10 minutes, sodium bisulfite modified at 64° C. for 2.5 hours, and stored at 4° C. for up to 20 hours. The sample is then mixed with 600 ul M-binding buffer and spun through the Zymo-Spin IC column for 30 seconds (>=10,000×g). The column is washed with 100 ul of M-Wash buffer, spun, and incubated in 200 ul of M-Desulphonation buffer for 15-20 minutes. The column is spun for 30 seconds (>=10,000×g), washed twice with 200 ul M-Wash buffer and spun at top speed. Then the sample is eluted from the column with 10 M-Elution buffer and stored in the freezer (−20° C.) prior to use in methylation assays.
  • Quantitative real-time RT-PCR (Method A):
  • After treatment with DNase I (Invitrogen, Carlsbad, Calif.), cDNA is synthesized from 3 ng of total RNA using Superscript II (Invitrogen). Real-time PCR is performed using SYBR Green PCR Core Reagents (PE Applied Biosystems, Foster City, Calif.) and an iCycler Thermal Cycler (Bio-Rad Laboratories, Hercules, Calif.). Quantitative RT-PCR is also performed using TaqMan probes and instrumentation (Applied Biosystems, Carlsbad, Calif.). The number of molecules of a specific cDNA in a sample is measured by comparing its amplification with that of standard samples containing 101 to 106 molecules. The expression levels in each sample are obtained by normalizing the number of its cDNA molecules with that of the GAPDH, actin, or other housekeeping genes.
  • Methylation-Specific Quantitative PCR (MS-QPCR):
  • Sodium-bisulfite modified DNA is PCR amplified in a final volume of 20 uL PCR buffer containing 10 mM Tris-HCl (pH8.3), 50 mM KCl, 2.5-4.5 mM MgCl2, 150-250 nM dNTPs, 0.2-0.4 uM primers, and 0.5 Units of AmpliTaq Gold polymerase (ABI) for an initial denaturation at 95° C. for 10 minutes followed by 45 cycles at 95° C.-15s, 55-66° C.-30s, 72° C.-30s, and a final extension at 72° C. for 7 minutes. Controls used to quantify methylation values include serially diluted methylated/unmethylated DNAs (Zymo) from 100% methylated to 0% methylated for each gene/CpG of interest, no-template control, reference gene (beta-actin) and standard curve of DNA quantity. Reactions are run using SYBR green (Roche) or methylation specific fluorescently labeled probes (ABI) on the ABI 7900HT Fast instrument with software to calculate standard curves and Ct values. Multiplex PCR can be evaluated in the same well for comparison when using fluorescently labeled methylated (FAM) and unmethylated (VIC) TaqMan (ABI) probes using the ABI 7900HT Fast instrument.
  • TABLE 14
    Target CpG Islands and Primers for Methylation Specific QPCR Primers
    (SEQ ID Nos. 285-311 (sense), SEQ ID Nos. 312-339 (antisense))
    Target ID Sense (5′-3′) Antisense (5′-3′)
    CD40_E58_R (M) GGGGTAGGGGAGTTAGTAGAGGTTTC CACTACAAAAACAAACGAACCATAACG
    CD40_E58_R (U) GGGGTAGGGGAGTTAGTAGAGGTTTT CACTACAAAAACAAACAAACCATAACAA
    COL1A2_E299_F(M) TAAGAAGTTAGTTTCGTGGTTACGT ACCCGAATCTACCCTATTTATACGAC
    COL1A2_E299_F(U) TAAGAAGTTAGTTTTGTGGTTATGT ACCCAAATCTACCCTATTTATACAAC
    DNMT3B_P352_R(M) GGGGTTTTGTTTTTTTTGAGTTTTC ACTCCTTCTAAAACCTTTTTCCCGA
    DNMT3B_P352_R(U) GGGGTTTTGTTTTTTTTGAGTTTTT ACTCCTTCTAAAACCTTTTTCCCAA
    EMR3_P39_R(M) ATGTAATTTTTAGGGTATTTTTTCG TCAAACTCATAATTCTACTTTTCGT
    EMR3_P39_R(U) ATGTAATTTTTAGGGTATTTTTTTG CATCAAACTCATAATTCTACTTTTCAT
    FRZB_P406_F(M) ATTTTATTTTCGGGAAGAGTAGTCG AAAAACCCCGCAAAACGT
    FRZB_P406_F(U) ATTTTATTTTTGGGAAGAGTAGTTG AAAAAACCCCACAAAAACAT
    GSTM2_P109_R(M) TTCGTTTTGGGTTTTTGGGC AAAAAAACCTTACTACGACCCCGC
    GSTM2_P109_R(U) TTTTTTGTTTTGGGTTTTTGGGTG AAAAAAAACCTTACTACAACCCCAC
    HOXA9_E252_R(M) TGTAGTTTTTAGTTTAAGGCGACGG AAACGCATATACCTACCGTCCGA
    HOXA9_E252_R(U) TGTAGTTTTTAGTTTAAGGTGATGG ACCAAAAACACATATACCTACCATCCAA
    HOXA9_P303_F(M) GGGTTTCGTTGGTCGTATTC CCATATATTTTTATATAAAAAAATCGTA
    HOXA9_P303_F(U) AGGGGTTTTGTTGGTTGTATTT AAACCATATATTTTTATATAAAAAAATCAT
    ITK_E166_R(M) TTTTTTTTCGAATTTTAAAGTTCG AAACTACTCACATACCCCATAACGA
    ITK_E166_R(U) TTTTTTTTGAATTTTAAAGTTTG AAACTACTCACATACCCCATAACAA
    KCNK4_E3_F(M) GGGTTTGGGAGATGTTAGATTAGC ACCAACCTTCTAACCTTAAACCGAA
    KCNK4_E3_F(U) GGTTTGGGAGATGTTAGATTAGTGT ACCAACCTTCTAACCTTAAACCAAA
    MT1A_E13_R(M) GGGTTTTATTAAGTTTTTTACGTGCG AAATCCATTTCGAACCGCGA
    MT1A_E13_R(U) TGGGTTTTATTAAGTTTTTTATGTGTG TTAAAATCCATTTCAAACCACAA
    PRSS8_E134_R(M) GCGGAGTTTAGTTAGTGGGC AAAACTAACCTCTAAAACAAAAAACGA
    PRSS8_E134_R(U) TGGTGGAGTTTAGTTAGTGGGTG CAAAACTAACCTCTAAAACAAAAAACAA
    RUNX3_E27_R(M) GAGTTTTTTTATTTTGGTTGTCGA TATACCCAAAAATTTAAATTCCCG
    RUNX3_E27_R(U) GGAGTTTTTTTATTTTGGTTGTTGA ATACCCAAAAATTTAAATTCCCAAT
    TNFSF8_E258_R(M) TAGGGTTGTAGTAAGTATTTAACGG CAACACCATAATAATAACCACCGTA
    TNFSF8_E258_R(U) ATGGATTTAGGGTTGTAGTAAGTATTTAAT CAACACCATAATAATAACCACCATA
  • TABLE 15
    Target CpG Islands and Primers for Bisulfite sequencing or MS-HRM and
    Reference Primers (SEQ ID Nos. 340-346 (sense), SEQ ID Nos. 347-353
    (antisense).
    Target ID Sense (5′-3′) Antisense (5′-3′)
    ITK_P114_F TGAGTTTATAGTTTTTTAAATATTATTTTA TACTCAAAAACAACTTACCTTCAAC
    ITK_E166_R TGTGTTAAGAGGTGATGTTTAAGGT AACAAATAAAACTACTCACATACCCC
    ITK_E166_R ATTAAGAAATTTTAATAAAAGAGAA TAAAACTACTCACATACCCCATAAC
    KIT_P405F-P367R TTTATTGTTTGGGGAGTATTTGGTAGGT CCACCTTTCCACCCCTAAAATATAAAC
    KLK10_P268_R GGAGATTGTAATAAATTAAGGTTAAAAGAG TAAAACACACACAAAACTCACTCAC
    MPO_P883_R TTATTAGAAGTTAAGAAGAAAGGGGAGTGA TACATCCAACAACCACCCAATAAAC
    Beta Actin TGGTGATGGAGGAGGTTTAGTAAGT AACCAATAAAACCTACTCCTCCCTTAA

    Table 16 lists CpG islands for either MS-QPCR or bisulfate sequencing.
  • TABLE 16
    Target ID
    CD40_E58_R
    COL1A2_E299_F
    DNMT3B_P352_R
    EMR3_P39_R
    FRZB_P406_F
    GSTM2_P109_R
    HOXA9_E252_R
    HOXA9_P303_F
    ITK_E166_R
    ITK_P114_F
    KCNK4_E3_F
    KIT_P367_R
    KIT_P405_F
    KLK10_P268_R
    MPO_P883_R
    MT1A_E13_R
    PRSS8_E134_R
    RUNX3_P247_F
    RUNX3_E27_R
    TNFSF8_E258_R
    • 6.15. Dysplastic Nevi vs. Benign Moles
  • Patients and Tissues:
  • Because dermatologists have difficulty distinguishing between benign moles and dysplastic nevi, an analysis was undertaken to find methylation markers for normal skin. Using the methods described above, profiling was performed on FFPE samples for dysplastic nevi (N=22) and benign non-dysplastic moles (N=34). The results are show below in Table 17.
  • TABLE 17
    Non-Dyplastic Dyplastic Mean
    Target ID Raw_p Bonf_p Mean β Mean β Δβ
    ALPL_P433_F 1.05E−05 0.01523 0.346 0.651 −0.305
    BCL6_P248_R 9.53E−06 0.01383 0.161 0.374 −0.213
    BDNF_E19_R 7.20E−06 0.01045 0.266 0.527 −0.261
    BDNF_P259_R 4.23E−06 0.00614 0.324 0.548 −0.224
    CD9_P585_R 7.04E−06 0.01021 0.225 0.440 −0.215
    CEACAM1_P44_R 2.53E−06 0.00367 0.375 0.652 −0.277
    CSPG2_P82_R 7.04E−06 0.01021 0.210 0.470 −0.259
    CTSD_P726_F 5.24E−06 0.00761 0.420 0.678 −0.258
    EFNB3_E17_R 4.47E−06 0.00648 0.388 0.605 −0.217
    EPHA2_P203_F 2.64E−05 0.03830 0.238 0.483 −0.245
    ERN1_P809_R 3.23E−06 0.00469 0.227 0.451 −0.224
    ETV1_P515_F 1.41E−06 0.00205 0.142 0.358 −0.216
    FANCE_P356_R 2.33E−06 0.00338 0.311 0.556 −0.244
    FGF2_P229_F 1.71E−06 0.00248 0.326 0.588 −0.261
    FGF9_P862_R 3.23E−06 0.00469 0.317 0.534 −0.217
    GAS7_P622_R 2.17E−06 0.00315 0.332 0.647 −0.315
    GDF10_E39_F 7.79E−06 0.01130 0.208 0.457 −0.249
    GFI1_E136_F 2.45E−05 0.03556 0.186 0.406 −0.221
    HDAC9_P137_R 7.14E−07 0.00104 0.126 0.352 −0.226
    HLA-DQA2_E93_F 1.24E−05 0.01800 0.665 0.887 −0.222
    HLA-DRA_P132_R 4.98E−06 0.00723 0.239 0.506 −0.266
    HTR2A_P853_F 1.97E−06 0.00286 0.112 0.363 −0.250
    IGF2AS_P203_F 2.36E−05 0.03422 0.275 0.524 −0.250
    IGFBP6_E47_F 1.97E−06 0.00286 0.366 0.615 −0.249
    IL16_P93_R 1.96E−05 0.02841 0.446 0.716 −0.270
    IPF1_P234_F 5.68E−06 0.00824 0.447 0.658 −0.211
    IPF1_P750_F 1.15E−05 0.01667 0.416 0.660 −0.244
    JUNB_P1149_R 2.98E−06 0.00432 0.147 0.360 −0.213
    KCNK4_E3_F 3.80E−06 0.00552 0.144 0.358 −0.215
    MAP3K8_P1036_F 1.68E−05 0.02443 0.330 0.586 −0.256
    MMP14_P13_F 2.64E−05 0.03830 0.199 0.473 −0.274
    MT1A_E13_R 1.41E−06 0.00205 0.217 0.425 −0.208
    NEU1_P745_F 2.12E−05 0.03073 0.160 0.369 −0.208
    NFKB1_P496_F 2.71E−06 0.00393 0.294 0.604 −0.310
    NGFB_P13_F 2.14E−06 0.00311 0.172 0.438 −0.266
    ONECUT2_E96_F 2.92E−07 0.00042 0.131 0.339 −0.209
    PCTK1_E77_R 1.30E−06 0.00188 0.536 0.737 −0.201
    PI3_P1394_R 4.31E−06 0.00626 0.569 0.784 −0.215
    PYCARD_P150_F 1.19E−06 0.00173 0.347 0.709 −0.362
    RET_seq_54_S260_F 1.68E−05 0.02443 0.147 0.420 −0.273
    RIPK1_P744_R 1.34E−05 0.01944 0.633 0.836 −0.202
    S100A4_E315_F 6.01E−07 0.00087 0.141 0.351 −0.210
    SEPT9_P374_F 4.23E−07 0.00061 0.096 0.314 −0.219
    TBX1_P885_R 3.51E−06 0.00509 0.147 0.356 −0.208
    TFF2_P178_F 6.01E−07 0.00087 0.540 0.816 −0.275
    TRIP6_P1090_F 2.84E−05 0.04124 0.171 0.384 −0.213
    VAV1_E9_F 1.96E−05 0.02841 0.379 0.612 −0.233
    • 6.16. ITK Staining Experiments
  • Immunofluorescence Staining for ITK (IL-2 inducible T-cell kinase).
  • Melanoma cell lines and cultured melanocytes were investigated for the presence of ITK protein using immunohistochemistry (IHC) with an antibody specific for ITK. Approximately fifty percent of 40 melanoma cell lines showed observable staining for ITK while no ITK staining was observed in the cultured primary melanocytes. IHC was also performed on primary melanoma tissue sections from patients.
  • In the primary tissue sections, the melanoma stained pink for ITK, while the surrounding normal skin does not stain for ITK. No other ITK staining was detected in the surrounding tissue and ITK staining was not detected in the normal melanocytes. Specifically, the section was stained with an antibody to ITK (abcam; 1:3000) with tyramide Cy5 amplification to visualize ITK (pink color). The specimen was also stained with the blue fluorescent stain DAPI (4′,6-diamidino-2-phenylindole) that binds strongly to A-T rich regions in DNA. A few ITK stained cells were seen at the dermal—epidermal junction extending out from the periphery of the tumor, likely representing migrating melanoma cells. These melanoma cells stained strongly for ITK, and the ITK-staining cells at the dermal-epidermal junction decrease in number as the distance increases from the melanoma. These were likely migrating melanoma cells and this information could be used for margin control at the time of surgery.
  • One of current markers for margin control, used primarily when melanomas are removed by MOHs surgery, is MART1 IHC staining. Alternatively, surgeons remove tissue based on an arbitrary distance from the tumor. MART1 is also expressed normal melanocytes so MART1 IHC staining shows the density and distribution of the melanocytes as an indicator of a clear margin. However, ITK IHC staining is present and then abruptly becomes absent at the edge of the tumor. ITK shows melanoma cells migrating along the basement membrane out from the tumor must be removed. ITK staining looks like it could be a better measure of clear margins.
  • Dual Fluorescent Immunohistochemistry (IF) and AQUA
  • Additionally, the ITK levels for three other melanomas and three nevi were studied quantitatively using Dual Fluorescent Immunohistochemistry and Automated Quantitative Analysis (AQUA) technology. Only melanocytic cells were quantitated using an S100 mask that defines the melanocytic region. To measure ITK levels in melanoma cells (defined by S100 staining) the consecutive dual fluorescent IHC was carried out in Bond Autostainer (Leica Microsystems Inc., Norwell Mass.). Slides were deparaffinized in Bond dewax solution (AR9222) and hydrated in Bond wash solution (AR9590). Antigen retrieval for ITK and 5100 was performed for 30 min at 1000 C in Bond-epitope retrieval solution 2 pH9.0 (AR9640). After pretreatment, slides were first incubated with ITK antibody (1:3000) followed with Bond polymer (DS9800); The tyramide Cy5 amplification was used to visualize ITK (PerkinElmer, Boston, Mass.). After completion of ITK staining the S100 antibody (Abcam 1:3200) was applied, which was detected with Alexa555 labeled goat anti rabbit secondary antibody (Invitrogen, Carlsbad, Calif.). The stained slides were mounted with ProLong Gold antifade reagent (Molecular Probes, Inc. Eugene, Oreg.) containing 4′,6-diamidino-2-phenylindole (DAPI) to define nuclei. All appropriate quality control stains (single and double) were carried out to make sure that there is no cross-reactivity between the antibodies.
  • Digitization of slides and AQUA
  • H&E stained whole tissue sections were digitally imaged (20× objective) using the Aperio ScanScope XT (Aperio Technologies, Vista, Calif.).
  • Aperio Fl./AQUA Image Analysis
  • Aperio Fl. (Aperio Inc) with integrated HistoRx AQUA technology (HistoRx, New Haven, Conn.) was used to scan the whole slides at ×20 objective through DAPI, CY3 and CY5 channels to identify nuclei, 5100 (mask) and ITK (target proteins) respectively. In whole tissue sections the 5100 positive areas within the tumor were annotated for each slide manually using positive pan tool; out of the focus or folded tissue areas were marked by negative pan to exclude from analysis. Annotated layers for each slide were submitted for analysis through spectrum software (Aperio Inc.) using AQUA clustering algorithm according to AQUAnalysis™ user guide: Aperio Edition (Rev. 1.0, CDN0044, HistoRx, New Haven, Conn.). Generated AQUA analysis data (summary of the AQUA scores and compartment masking produced by AQUA) was pushed back to spectrum and exported as csv file.
  • PM2000/AQUA Image Analysis
  • To validate AQUA scores obtained through Aperio Fla., the high resolution acquisition was performed in PM2000 (HistoRx) as well. The same areas, analyzed in Aperio-FL were acquired in PM2000 for scoring the ITK expression in S100 mask. The marked images were analyzed by AQUA® software version #2.2 using HistoRx AQUA clustering algorithm. Analysis profile and merged images were generated for each slide. Spots, which didn't pass the validation, were excluded from analysis.
  • The results (Table 18) demonstrated that ITK is observable in the melanomas and lower in the nevi (moles), as denoted by the Aqua Score that measures expression within the melanocytic region and excludes keratinocyte, fibroblast and other non-melanocytic cell staining. Further staining of normal skin section showed no significant ITK expression in melanocytes within the normal skin.
  • TABLE 18
    Aperio FL Average of Target in
    Sample Tumor Mask AQUA score
    Melanoma 1 418
    Melanoma 2 262
    Melanoma 3 268
    Melanoma 4 325
    Nevus (mole) 1 147
    Nevus (mole) 2 191
    Nevus (mole) 3 34
    Normal skin (melanocytes) 4
  • It is to be understood that, while the invention has been described in conjunction with the detailed description, thereof, the foregoing description is intended to illustrate and not limit the scope of the invention. Other aspects, advantages, and modifications of the invention are within the scope of the claims set forth below. All publications, patents, and patent applications cited in this specification are herein incorporated by reference as if each individual publication or patent application were specifically and individually indicated to be incorporated by reference.
  • This application contains a sequence listing. It has been submitted electronically via EFS-Web as an ASCII text file entitled “UNC10001WO-Sequence— Listing_ST25.txt”. The sequence listing is 68 kilobytes in size, and was created on Sep. 12, 2011. It is hereby incorporated by reference in its entirety.

Claims (43)

What is claimed is:
1. A method for detecting melanoma in a tissue sample which comprises:
(a) measuring a level of methylation of one or more regulatory elements differentially methylated in melanoma and benign nevi; and
(b) determining whether melanoma is present or absent in the tissue sample.
2. The method of claim 1, wherein the level of methylation is measured at single CpG site resolution.
3. The method of claim 1, wherein the tissue sample is a common nevi sample.
4. The method of claim 1, wherein the tissue sample is a dysplastic nevi sample.
5. The method of claim 1, wherein the tissue sample is a benign atypical nevi sample.
6. The method of claim 1, wherein the tissue sample is a melanocytic lesion of unknown potential.
7. The method of claim 1, wherein the tissue sample is a formalin-fixed, paraffin-embedded sample.
8. The method of claim 1, wherein the tissue sample is a fresh-frozen sample.
9. The method of claim 1, wherein the tissue sample is a fresh tissue sample.
10. The method of claim 1, wherein the tissue sample is a dissected tissue, an excision biopsy, a needle biopsy, a punch biopsy, a shave biopsy, a strip biopsy, or a skin biopsy sample.
11. The method of claim 1, wherein the tissue sample is a lymph node biopsy sample.
12. The method of claim 1, wherein the lymph node biopsy sample is a sentinel lymph node sample.
13. The method of claim 1, wherein the tissue sample is a sample from a cancer metastasis.
14. The method of claim 1, wherein the regulatory elements are regulatory elements associated with immune response/inflammatory pathway genes, hormonal regulation genes, or cell growth/cell adhesion/apoptosis genes.
15. The method of claim 1, wherein the regulatory elements are regulatory elements associated with a gene encoding CARD15, CCL3, CD2, EMR3, EVI2A, FRZB, GSTM2, HLA-DPA1, IFNG, ITK, KCNK4, KLK10, LAT, MPO, NPR2, OSM, PSCA, PTHLH, PTHR1, RUNX3, TNFSF8 or TRIP6.
16. The method of claim 15, wherein hypermethylation of the regulatory elements associated with a gene encoding FRZB, GSTM2, KCNK4, NPR2, or TRIP6 is indicative of melanoma.
17. The method of claim 15, wherein hypomethylation of the regulatory elements associated with a gene encoding CARD15, CCL3, CD2, EMR3, EVI2A, HLA-DPA1, IFNG, ITK, KLK10, LAT, MPO, OSM, PSCA, PTHLH, PTHR1, RUNX3 or TNFSF8 is indicative of melanoma.
18. The method of claim 1, wherein the level of methylation is measured using a bisulfate conversion-based microarray assay.
19. The method of claim 1, wherein the level of methylation is measured using a differential hybridization assay.
20. The method of claim 1, wherein the level of methylation is measured using a methylated DNA immunoprecipitation based assay.
21. The method of claim 1, wherein the level of methylation is measured using a methylated CpG island recovery assay.
22. The method of claim 1, wherein the level of methylation is measured using a methylation specific polymerase chain reaction assay.
23. The method of claim 1, wherein the level of methylation is measured using a methylation sensitive high resolution melting assay.
24. The method of claim 1, wherein the level of methylation is measured using a microarray assay.
25. The method of claim 1, wherein the level of methylation is measured using a pyrosequencing assay.
26. The method of claim 1, wherein the level of methylation is measured using an invasive cleavage amplification assay.
27. The method of claim 1, wherein the level of methylation is measured using a sequencing by ligation based assay.
28. The method of claim 1, wherein the level of methylation is measured using a mass spectrometry assay.
29. The method of claim 1, further comprising evaluating the quality of the sample by measuring the levels of skin specific markers.
30. The method of claim 29, wherein the skin specific markers are measured by antibody staining, differential methylation, expression analysis, or fluorescence in situ hybridization (FISH).
31. The method of claim 1, further comprising staining the tissue sample with one or more antibodies.
32. The method of claim 31, wherein the antibodies are 5100, gp100 (HMB-45 antibody), MART-1/Melan-A, MITF, or tyrosinase antibodies.
33. The method of claim 32, wherein the antibodies are a cocktail of gp100 (HMB-45 antibody), MART-1/Melan-A, and tyrosinase antibodies.
34. The method of claim 1, further comprising fluorescence in situ hybridization (FISH), comparative genomic hybridization (CGH), or gene expression analysis.
35. The method of claim 1, wherein the regulatory element differentially methylated has a sensitivity analysis area under the curve of greater than 0.70.
36. The method of claim 1, wherein the regulatory element differentially methylated has a sensitivity analysis area under the curve of greater than 0.85.
37. The method of claim 1, wherein the regulatory element differentially methylated has a sensitivity analysis area under the curve of greater than 0.98.
38. The method of claim 1, wherein a plurality of regulatory elements differentially methylated are measured, and together they have a sensitivity analysis area under the curve of greater than 0.99.
39. The method of claim 1, wherein the levels of methylation for 4 or more regulatory elements are measured.
40. The method of claim 1, wherein the levels of methylation for 8 or more regulatory elements are measured.
41. The method of claim 1, wherein the levels of methylation for 12 or more regulatory elements are measured.
42. A kit comprising:
(a) at least one reagent selected from the group consisting of:
(i) a nucleic acid probe capable of specifically hybridizing with a regulatory element differentially methylated in melanoma and benign nevi;
(ii) a pair of nucleic acid primers capable of PCR amplification of a regulatory element differentially methylated in melanoma and benign nevi; and
(iii) a methylation specific antibody and a probe capable of specifically hybridizing with a regulatory element differentially methylated in melanoma and benign nevi; and
(b) instructions for use in measuring a level of methylation of at least one regulatory element in a tissue sample from a subject suspected of having melanoma.
43. A method of identifying a compound that prevents or treats melanoma progression, the method comprising the steps of:
(a) contacting a compound with a sample comprising a cell or a tissue;
(b) measuring a level of methylation of one or more regulatory elements differentially methylated in melanoma and benign nevi; and
(c) determining a functional effect of the compound on the level of methylation; thereby identifying a compound that prevents or treats melanoma.
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